rs2248372 in HCP5 gene and ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO

PMID 20041166 2009 Common genetic variation and the control of HIV-1 in humans.

PMID 21051598 2010 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.

rs2248372 in HCP5 gene and AIDS, PROGRESSION TO

PMID 20041166 2009 Common genetic variation and the control of HIV-1 in humans.

PMID 21051598 2010 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.

rs2284178 in HCP5 gene and Acquired Immunodeficiency Syndrome

PMID 19115949 2009 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).

rs3131643 in HCP5 gene and Blood basophil count (lab test)

PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs9281492 in HCP5 gene and Body Height

PMID 28552196 2017 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.

rs116822326 in HCP5 gene and Carcinoma of lung

PMID 28604730 2017 Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.

rs2395029 in HCP5 gene and Chemical and Drug Induced Liver Injury

PMID 19483685 2009 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.

PMID 30661239 2019 Drug-Induced Liver Injury due to Flucloxacillin: Relevance of Multiple Human Leukocyte Antigen Alleles.

rs114277634 in HCP5 gene and Child Development Disorders, Pervasive

PMID 28540026 2017 Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.

rs6940467 in HCP5 gene and Coronary heart disease

PMID 21971053 2012 Genome-wide association study of coronary artery disease in the Japanese.

rs2248373 in HCP5 gene and Corpuscular Hemoglobin Concentration Mean

PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs12660382 in HCP5 gene and Diabetes Mellitus, Insulin-Dependent

PMID 17632545 2007 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.

rs79022003 in HCP5 gene and Eosinophil count procedure

PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs2248372 in HCP5 gene and HIV-1, RESISTANCE TO

PMID 20041166 2009 Common genetic variation and the control of HIV-1 in humans.

PMID 21051598 2010 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.

rs2248372 in HCP5 gene and HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO

PMID 20041166 2009 Common genetic variation and the control of HIV-1 in humans.

PMID 21051598 2010 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.

rs114864815 in HCP5 gene and Herpes zoster disease

PMID 25297839 2015 Genetic variation in the HLA region is associated with susceptibility to herpes zoster.

PMID 30298529 2019 The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.

rs2395488 in HCP5 gene and Lupus Erythematosus, Systemic

PMID 24871463 2014 GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.

rs3131643 in HCP5 gene and Lymphocyte Count measurement

PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs2844507 in HCP5 gene and Multiple Sclerosis

PMID 17660530 2007 Risk alleles for multiple sclerosis identified by a genomewide study.

rs114012716 in HCP5 gene and Myositis

PMID 26291516 2015 Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes.

rs12660382 in HCP5 gene and Pemphigus Vulgaris

PMID 22437316 2012 Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris.

rs3094013 in HCP5 gene and Physical Activity Measurement

PMID 28448500 2017 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.

rs2523673 in HCP5 gene and Platelet Count measurement

PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs3094013 in HCP5 gene and Polymyositis

PMID 26362759 2016 Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups.

rs2395029 in HCP5 gene and Psoriasis

PMID 18369459 2008 However, rs2395029 encoding the G2V polymorphism within the class I gene HCP5 (combined P = 2.13x10(-26) in U.S. cases) yielded the highest ORs with both PS and PSA (4.1 and 3.2 respectively).

rs12660382 in HCP5 gene and 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.

rs114277634 in HCP5 gene and Schizophrenia

PMID 28540026 2017 Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.

rs116822326 in HCP5 gene and Squamous cell carcinoma of lung

PMID 28604730 2017 Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.