Variant: rs1980493

present in Gene: BTNL2;TSBP1-AS1 present in Chromosome: 6 Position on Chromosome: 32395438 Alleles of this Variant: T/C

rs1980493 in BTNL2;TSBP1-AS1 gene and Anti-cyclic citrullinated peptide antibody PMID 19287509 2009 Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis.

rs1980493 in BTNL2;TSBP1-AS1 gene and Anti-cyclic citrullinated peptide antibody level PMID 19287509 2009 Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis.

rs1980493 in BTNL2;TSBP1-AS1 gene and Autoimmune thyroiditis PMID 25936594 2015 Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes.

rs1980493 in BTNL2;TSBP1-AS1 gene and Diabetes Mellitus, Insulin-Dependent PMID 17632545 2007 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.

PMID 25936594 2015 Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes.

rs1980493 in BTNL2;TSBP1-AS1 gene and Frontotemporal dementia PMID 24943344 2014 Frontotemporal dementia and its subtypes: a genome-wide association study.

rs1980493 in BTNL2;TSBP1-AS1 gene and Lupus Erythematosus, Systemic PMID 24871463 2014 GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.

rs1980493 in BTNL2;TSBP1-AS1 gene and Membranous glomerulonephritis PMID 21323541 2011 Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.

rs1980493 in BTNL2;TSBP1-AS1 gene and Myasthenia Gravis PMID 23055271 2012 Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.

rs1980493 in BTNL2;TSBP1-AS1 gene and Rheumatoid Arthritis PMID 21156761 2011 A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis.

PMID 19503088 2009 REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.

PMID 17804836 2007 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.