rs7980288 in A2M;KLRG1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12321593 in AACS gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9893173 in ABCA9 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1517284 in ABCC9 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs687621 in ABO gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30395268 2018 Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.

rs11851603 in ACIN1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4848366 in ACOXL gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1551568 in ACSM1;ACSM3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10952242 in ACTR3C gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6451032 in ADAMTS12 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17163154 in ADAMTS19 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12516283 in ADAMTS6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7175718 in ADAMTSL3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7704053 in ADCY2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2501574 in ADD3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17598910 in ADGRA3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2802684 in ADGRB3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4449617 in ADGRF5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6570507 in ADGRG6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30395268 2018 Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs7079515 in ADK gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6745099 in AFF3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12695894 in AGTR1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16900846 in AHRR gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2004962 in AK5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9384713 in AK9 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9303973 in AKAIN1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3784169 in AKAP6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1729549 in AKAP7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17133680 in AKR1E2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7165301 in ALDH1A2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16837171 in ALDH1L1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7539517 in ALG14 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8086790 in ALPK2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17045918 in ANK2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16915102 in ANK3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7580108 in ANKRD44-IT1;ANKRD44 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12579350 in ANO2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2138050 in ANO4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs34762579 in AP1AR gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs25673 in AP3D1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6559648 in APBA1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16942981 in AQP4-AS1;CHST9 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12029076 in ARF1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs17654410 in ARHGAP42 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2317440 in ARHGEF3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17036090 in ARHGEF38 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7169055 in ARNT2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2034669 in ASB18 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs140147 in ASCC2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2089164 in ASIC2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1335415 in ASTN2;LOC105376237 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16849542 in ATF6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7633661 in ATP2B2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7239484 in ATP8B1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17653487 in ATXN10 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11063544 in B4GALNT3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3784008 in BATF gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17170187 in BBS9 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41347145 in BCAT2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4940576 in BCL2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 26394188 2015 Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls.

PMID 28334814 2017 Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis.

rs11177789 in BEST3;LOC105369823 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16963833 in BFAR gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10756785 in BNC2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30395268 2018 Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.

PMID 26211971 2015 A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis.

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs73235136 in BOC gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs1570032 in BPIFA3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16892391 in BST1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10748574 in BTAF1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17039266 in BTBD11 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8064088 in C16orf70 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11681143 in C2orf27A gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6826964 in C4orf19 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7215018 in CA10 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11062098 in CACNA1C gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17156195 in CACNA2D1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs860010 in CALN1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17781645 in CAND1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs214321 in CAPZB gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12378451 in CARD19;LOC101927993 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6671070 in CCDC18 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1583333 in CCDC26 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4801109 in CCDC68 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11049656 in CCDC91 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17002460 in CCNG2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6488336 in CD163L1;CD163 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4891786 in CD226 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7612956 in CD96;LOC105374039 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6897209 in CDC42SE2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2194285 in CDH13 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

PMID 30395268 2018 Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.

rs7232172 in CDH2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8092627 in CDH7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16942585 in CDH8 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17124679 in CDK5RAP1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17694493 in CDKN2B-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4920894 in CDO1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11257029 in CELF2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10930328 in CERS6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2833908 in CFAP298-TCP10L;TCP10L gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13269361 in CHD7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11129708 in CHL1-AS1;CHL1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7782730 in CHN2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17768858 in CHODL gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16971721 in CHP1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs203351 in CIT gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4514513 in CLEC2B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12416741 in CLPB gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11921493 in CMC1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17029445 in CMTM7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41444048 in CNNM1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13290451 in CNTFR;CNTFR-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs2779767 in CNTLN gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2530313 in CNTNAP2;LOC105375554 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3793821 in COL13A1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17052419 in COL23A1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2046158 in COL24A1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9894591 in COX10-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41520848 in CPSF1P1;SLC5A4-AS1;SLC5A4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7672202 in CRACD gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6538452 in CRADD gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs160335 in CREB5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs7199790 in CRNDE;LOC101927480 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10405809 in CRX gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs5996945 in CRYBB2P1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs545608 in CRYZL2P-SEC16B;SEC16B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs11136775 in CSMD1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs34742539 in CSMD3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41336052 in CTIF gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1670140 in CTNNA3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4745925 in CTNNA3;LRRTM3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7537879 in CTNNBIP1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10059423 in CTNND2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1039751 in CWC15 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1436931 in CXCL12 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3091344 in CYB5R3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3754260 in DAB1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12037261 in DAB1;LOC105378746 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16824134 in DAW1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1346972 in DCC gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16949906 in DCT gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs217373 in DDX56 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8028238 in DENND4A gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3737 in DEPDC4;ACTR6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7835803 in DEPTOR gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13343081 in DGAT2L6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1981680 in DGKB gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7096725 in DIP2C gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs797487 in DLEU1;DLEU7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10466716 in DLG2;DLG2-AS2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10915816 in DNAH14 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3890771 in DNAH6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9380815 in DNAH8 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4364959 in DNAJC1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1451050 in DNAJC24 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10839572 in DNHD1;RRP8 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2805495 in DNMBP;DNMBP-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9794336 in DOCK1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7729471 in DOCK2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2659584 in DOCK5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12353411 in DOCK8 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6023383 in DOK5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7160830 in DPF3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10195136 in DPP10 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11167990 in DPYSL3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4337094 in DRAM1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2835750 in DYRK1A gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2698744 in ECT2L gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6822565 in EDNRA gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7785013 in EGFR gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2254958 in EIF2AK2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10799667 in EIF4G3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4762293 in ELK3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1809803 in ENOX1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9321309 in ENPP3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2247732 in EPB41L1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6871057 in ERBIN gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10988944 in ERP44 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16827201 in ERVMER61-1;LOC105371656 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11117615 in ESRRG gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17618877 in EXPH5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4810619 in EYA2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12211518 in EYS gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2286490 in FAM126A gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1018597 in FAM155A gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs511875 in FAM183A gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3891620 in FBH1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6463483 in FBXL18 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4315757 in FBXW7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11920657 in FHIT gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4627442 in FHOD3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs565418 in FMO10P gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1442502 in FMO8P gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17153734 in FRMD4A gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12833832 in FRMPD4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12149832 in FTO gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1361728 in FYB2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1875119 in FZD10-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10122943 in GABBR2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs493971 in GABPB1;MIR4712;GABPB1-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10238767 in GALNT11 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12435957 in GALNT16 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1794735 in GATC gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6800135 in GBE1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17094393 in GFRA1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4723038 in GHRHR gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6802807 in GLB1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs890832 in GLRA1;LOC112267935 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10869925 in GNA14;GNA14-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2774316 in GNG4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10919410 in GORAB-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11813054 in GOT1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17103572 in GPHN gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9487264 in GPR63 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1568506 in GRB14 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11201942 in GRID1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2616673 in GRID1;GRID1-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2832402 in GRIK1;BACH1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs480495 in GRIK3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16966656 in GRIN2A gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11709369 in GRIP2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11020496 in GRM5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13353402 in GRM7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4727364 in GSAP gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17036152 in GSTCD;INTS12 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10890627 in GUCY1A2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17629956 in GUSBP11 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12498100 in H3P12;LINC01205 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2124373 in HPS5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1518814 in HSD17B12 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10489629 in IL23R;C1orf141 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17636964 in IPMK gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6964752 in IQCE gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs890195 in IRF2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2925763 in ITGB6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17455862 in ITGB8 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2180369 in ITPK1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11981911 in JAZF1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13257503 in JPH1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16853497 in KAZN gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11180340 in KCNC2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6826348 in KCNIP4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16839682 in KCNT2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7025832 in KDM4C gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11105952 in KERA gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41337248 in KIAA0513 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9921758 in KIAA0556 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12263288 in KIAA1217 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs767434 in KIAA1324L gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7862229 in KIAA2026 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs238282 in KIF1C;KIF1C-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs188915802 in KIF24;SERPINH1P1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs1024036 in KIF9 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2025424 in KLF12 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1814813 in KLHL2P1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7953558 in KLRD1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs680832 in L3MBTL4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9621705 in LARGE1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1482465 in LARS2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs663599 in LATS2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs678741 in LBX1-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 26394188 2015 Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls.

PMID 28334814 2017 Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis.

rs514438 in LCMT2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1785123 in LDLRAD4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17059596 in LHFPL6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7908284 in LHPP gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3135977 in LIG3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10177451 in LINC00298 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9541841 in LINC00383 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2496411 in LINC00437 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12765688 in LINC00595 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2427394 in LINC00686 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7918642 in LINC00840 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2139709 in LINC00882 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7204525 in LINC00922 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2140629 in LINC01006 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4833941 in LINC01091 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10175478 in LINC01122 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7627798 in LINC01192 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2193790 in LINC01317 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10884569 in LINC01435 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2207195 in LINC01524;LOC105372666 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17138199 in LINC01570;RBFOX1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs28409621 in LINC01605 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17629735 in LINC01612 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7593846 in LINC01798 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 28334814 2017 Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis.

rs16825105 in LINC01807 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4912575 in LINC01839 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1388100 in LINC02026 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41421845 in LINC02119;LINC02107 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4949146 in LINC02165 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17440304 in LINC02201 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6877715 in LINC02215 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8015760 in LINC02306 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17126879 in LINC02331 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16942927 in LINC02336;LOC107984621 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17116329 in LINC02346 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1019348 in LINC02405 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2060546 in LINC02410;LOC105369921 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17032384 in LINC02456;HELLPAR gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10858818 in LINC02458 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16893677 in LINC02542 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11023018 in LINC02683 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11036663 in LINC02745 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10789869 in LINC02762 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17269348 in LIPC gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1214467 in LIPK gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11505688 in LOC100133091 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1028911 in LOC100506207;HULC gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7645307 in LOC100507291 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs602651 in LOC101927026 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7713414 in LOC101927421;LINC02240 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs881972 in LOC101927872 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1922003 in LOC101928278 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs276961 in LOC101928582 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs141903557 in LOC101928978 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs4697584 in LOC101929161 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs744617 in LOC102723657 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7864098 in LOC102723803 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11921904 in LOC102724419 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1887604 in LOC102724520 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17020436 in LOC102724542 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs475796 in LOC102724632;CBFA2T3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1839261 in LOC102724710 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1431015 in LOC102724858 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6538505 in LOC102724960 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs36130286 in LOC105369165 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3019536 in LOC105369325 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10843459 in LOC105369649 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10783853 in LOC105369783;CTDSP2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17031683 in LOC105369938;MYBPC1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2161877 in LOC105370003 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9671744 in LOC105370604 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1462268 in LOC105370651 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1918505 in LOC105370802 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17712720 in LOC105370826 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12050567 in LOC105370982 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30395268 2018 Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.

rs13330098 in LOC105371078 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs142502288 in LOC105371497 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs10436911 in LOC105371657 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs726502 in LOC105371731 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8071545 in LOC105371896 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2145839 in LOC105372648 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2831758 in LOC105372764 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4603874 in LOC105373032 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9626886 in LOC105373075 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs5767109 in LOC105373081 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12086567 in LOC105373108 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11896635 in LOC105373831;PLCL1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16847364 in LOC105374126 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11134225 in LOC105374645 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2881493 in LOC105375268 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4562194 in LOC105375322 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41492347 in LOC105375630 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1352557 in LOC105375716 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1454618 in LOC105375746 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16905897 in LOC105375911 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10959745 in LOC105375974 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16937559 in LOC105375988 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7029953 in LOC105376020 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11139622 in LOC105376110;LOC107987087 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs200549 in LOC105376253 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs548732 in LOC105376471 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2883217 in LOC105377378 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4334701 in LOC105377462 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30395268 2018 Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.

rs17022539 in LOC105377476 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41462346 in LOC105377488 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6748662 in LOC105377632 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11136965 in LOC105377797 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs323237 in LOC105377862 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16889666 in LOC105377865 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2750030 in LOC105377901 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs246478 in LOC105378234 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17100759 in LOC105378516 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17093334 in LOC105378798 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12074373 in LOC105378930 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1114783 in LOC105379102 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12656223 in LOC105379163;MARCHF3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16965217 in LOC107983981 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6069391 in LOC107984001 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2147744 in LOC107984274 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11019401 in LOC107984371 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11830166 in LOC107984525 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1548654 in LOC107984526;IFNG-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9972050 in LOC107984602 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4899339 in LOC107984686;LOC646548 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs654642 in LOC107985126 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2827352 in LOC107985508 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2834613 in LOC107985515;LINC00160 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10432510 in LOC107985833 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13387240 in LOC107985955 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6730483 in LOC107985961 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10170968 in LOC107985969 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17073759 in LOC107986018;MAGI1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4895110 in LOC107986108 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10019193 in LOC107986198;DDX60L;PALLD gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17038704 in LOC107986324;LINC02233 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4916753 in LOC107986387 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2179803 in LOC107986603;TRAM2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs971199 in LOC107986606 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1231498 in LOC107986623 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs886448 in LOC107986777 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13249487 in LOC107986891 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11997538 in LOC107986943 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7871426 in LOC107987037 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10867194 in LOC107987083 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7020497 in LOC107987088 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10739217 in LOC107987108 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs658839 in LOC112267962 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs2374916 in LOC112268050 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2830622 in LOC112268279 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10514207 in LOC339298 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10017335 in LOC645513 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7007550 in LONRF1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9645995 in LRCH1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7923176 in LRMDA gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1875163 in LRMDA;LOC105378367 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41497646 in LRP1B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4612793 in LRRC4C gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs285460 in LRRC52-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11984462 in LRRC6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12062605 in LRRC7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7709505 in LUCAT1;LOC107986433 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1562263 in LUZP2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13198304 in LY86-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1027986 in LYN gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs703254 in MACROH2A1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11161318 in MAGEL2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7633294 in MAGI1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 28334814 2017 Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis.

rs41518446 in MAML2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16964720 in MAPK6;LOC112268150 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16966292 in MAPRE2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41445146 in MARCHF1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16962779 in MBTPS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12638707 in MCF2L2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17149197 in ME3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11852650 in MEIS2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17712868 in METTL25 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6804758 in MFN1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17072594 in MFSD4B;REV3L gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2352036 in MGC27382;PTGFR gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4149202 in MGST1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7102350 in MIR192;MIR194-2HG;MIR194-2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6472873 in MIR2052HG gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs859711 in MIR29B2CHG gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6709385 in MIR3681HG gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1828853 in MIR4300HG gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 29016859 2017 A functional variant in MIR4300HG, the host gene of microRNA MIR4300 is associated with progression of adolescent idiopathic scoliosis.

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs583635 in MIR548B;FAM184A gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16983616 in MIR646HG gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2057805 in MLKL gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12479345 in MMADHC-DT gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7935375 in MMP26 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13221118 in MNX1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6670122 in MRPL24 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1905041 in MSC-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1059214 in MSMO1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8055724 in MT1L gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11205303 in MTMR11 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs3899582 in MTUS2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2682204 in MYLK gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs820343 in MYLK;LOC105369194 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9284241 in MYO16 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7292706 in MYO18B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1947457 in MYO1B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4797102 in MYOM1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16824453 in NAALADL2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs621332 in NALCN gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1430797 in NBAS gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4675317 in NBEAL1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11240095 in NBPF13P;LOC728989 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10120294 in NDUFA8 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2161199 in NDUFAF2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10741881 in NELL1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16906991 in NELL1;LOC105376585 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10748401 in NELL2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1942462 in NETO1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16996066 in NFATC2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs192668 in NIPBL gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41334545 in NLGN1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2037955 in NOD1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16913221 in NOX4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2866784 in NPNT gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs183350 in NPRL3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2472670 in NR1I2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7167152 in NR2F2-AS1;LOC112268156 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2816992 in NR5A2;LOC107985244 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7722878 in NREP gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17559044 in NRG3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41522849 in NRXN1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11015020 in NSUN6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs482012 in NT5DC1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs3785961 in NUFIP2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10141031 in NUMB gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7547924 in ODR4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2602813 in OPCML gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6587444 in OR2T33 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2955821 in OR3A2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12380216 in OR7E108P gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1107643 in OSBPL10 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11019290 in OSBPL9P3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9776186 in OSTF1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41485546 in OTX2-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7320453 in PAN3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6689901 in PAPPA2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12694012 in PARD3B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17248887 in PARM1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8027881 in PARP16;LOC112268147 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1180949 in PARS2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11207881 in PATJ gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16863633 in PAX3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1962471 in PCAT1;CASC21 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4935555 in PCDH15 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41530644 in PCDH7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9529199 in PCDH9 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2273673 in PCNX2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12701204 in PDE1C gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10493390 in PDE4B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10052657 in PDE4D gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4124921 in PDE4DIP gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3799385 in PDE7B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7657225 in PDGFC gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11015260 in PDSS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6878827 in PDZD2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7772565 in PHACTR2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4882970 in PHC1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17710886 in PKD1L1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17130220 in PKN2-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16825225 in PLCH1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7653834 in PLCL2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17011903 in PLXNA2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3803070 in PLXNC1;CEP83 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1771200 in POMP gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs687706 in PPARGC1A gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9520222 in PPIAP24 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10409138 in PPP1R37;MARK4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4624724 in PPP2R2C gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3783747 in PPP2R5E gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12289095 in PRCP gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs729663 in PREX1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs696021 in PRICKLE2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1483186 in PRKCD gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1536014 in PRKCH gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41332544 in PRKG2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2077934 in PRKN gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8133217 in PRMT2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10086956 in PSKH2;ATP6V0D2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17138613 in PTER gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6729895 in PTH2R;LOC101927960 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2784598 in PTPRD gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1768353 in PTPRK gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7802459 in PTPRN2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4830580 in PUDP gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16916544 in PXDNL gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs856134 in PYHIN1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9955120 in RAB12 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6431549 in RAB17;LOC105373958 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3769050 in RAMP1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13337052 in RBFOX1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17495047 in RELL1;C4orf19 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6965019 in RELN gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4340104 in RERGL gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17658908 in RFX3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8751 in RHOBTB3;GLRX gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7216187 in RHOT1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2807510 in RIMS1;LOC107986611 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41439051 in RIT2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41337747 in RNF150 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6913494 in ROS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16861629 in RPL39L gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7090135 in RPS24 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs645078 in RPS6KA4;MIR1237 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2018199 in RSL1D1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9680823 in RTCB gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2797436 in RYR2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11072541 in RYR3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11042561 in SBF2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs418635 in SBF2;SBF2-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9293749 in SCAMP1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs519238 in SCARA3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9883498 in SCHIP1;IQCJ-SCHIP1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17166189 in SCIN;LOC107986769 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9400146 in SCML4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs302121 in SEMA3E gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs363656 in SEMA4F gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3985863 in SEMA6D gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8074026 in SERPINF2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11901421 in SESTD1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17171238 in SFRP4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17120351 in SGCZ gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9493877 in SGK1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs739496 in SH2B3;ATXN2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10910445 in SIPA1L2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1595459 in SIRPB3P gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8080031 in SKAP1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2612539 in SLC14A2;SLC14A2-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17025736 in SLC16A4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7870850 in SLC24A2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1887489 in SLC24A2;LOC105375988 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17689531 in SLC4A4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41441744 in SLC5A4;SLC5A4-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs301696 in SLC9C2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4762694 in SLCO1B3-SLCO1B7;SLCO1B7 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11170829 in SMUG1-AS1;SMUG1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9643689 in SNTG1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3902080 in SNX29 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6461309 in SNX8 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6446592 in SORCS2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10884064 in SORCS3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2470907 in SORD2P gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1455114 in SOX6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30395268 2018 Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.

rs17813412 in SPAG16 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs295145 in SPATS2L gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6737027 in SPDYA gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6591177 in SPDYC gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7175472 in SPRED1;LOC107984760 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6581526 in SRGAP1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs446064 in SSBP2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10782606 in ST6GALNAC3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8093234 in ST8SIA5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7138824 in STAB2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2764627 in STARD13;STARD13-AS gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11827790 in STIM1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11146304 in STK32C gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7358633 in STK38L gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11097592 in STPG2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10017573 in STX18 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16955527 in STXBP4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17076671 in STXBP5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1225764 in SYCP2L gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs450277 in SYN2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17031729 in SYNPR;SYNPR-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1491744 in TAFA1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs455049 in TANGO2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4597312 in TANGO6 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6992733 in TBC1D31 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41384544 in TBC1D5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1978060 in TBX1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 31417091 2019 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.

rs2937582 in TENM2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17073715 in TENM3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3814284 in TENT4B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1441357 in THSD4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11139357 in TLE1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12569424 in TLL2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11466648 in TLR10 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11536869 in TLR4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4911198 in TM9SF4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1578957 in TMEM131 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7686062 in TMEM131L gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12371559 in TMEM132C gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11235059 in TMEM135 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs5942618 in TMEM164 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6752950 in TMEM182 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41508744 in TMEM252-DT gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1883758 in TMEM51 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41320847 in TMIGD3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1283198 in TMTC4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9810566 in TNIK;LOC105374216 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 28334814 2017 Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis.

rs113654 in TOX gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs3757384 in TPI1P2;TNPO3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11157436 in TRAV30 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17065840 in TSC22D1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16822427 in TSEN15 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6022494 in TSHZ2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4332347 in TSNAX-DISC1;DISC1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs35097 in TSPAN11 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17027607 in TSPAN5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1528706 in UNC5D gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1413151 in USP26 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4530873 in UTRN gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41528652 in UTS2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1254900 in VAMP5 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7311856 in VDR gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs10967100 in VLDLR-AS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs730819 in VPS16;PTPRA gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs616346 in VPS37C gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs7150701 in WARS1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17011373 in WDFY4;LRRC18 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6675269 in WDR26 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1051432 in WDR59 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1175646 in WNT2B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs41520844 in WRN gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs34592201 in WWOX gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs5974155 in XACT gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16860928 in XCL1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9291 in YY1;SLC25A29 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2367177 in ZDHHC15 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2842509 in ZFAND3 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1046774 in ZMAT1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs4472504 in ZMAT4 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs17206080 in ZNF254 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs16866800 in ZNF385B gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9921634 in ZNF423 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs1027341 in ZNF438 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs12459057 in ZNF536 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs8111296 in ZNF723 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs9838540 in ZPLD1 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.