Variant: rs2187668 

    present in Gene: LOC107986589;HLA-DQA2;HLA-DQA1
    present in Chromosome: 6
    Position on Chromosome: 32638107
    Alleles of this Variant: C/T

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Adenocarcinoma of lung (disorder) PMID 19836008 2009 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Asthma PMID 21150878 2011 Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Autoimmune Chronic Hepatitis PMID 24768677 2014 Genome-wide association study identifies variants associated with autoimmune hepatitis type 1.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Autoimmune Hepatitis with Centrilobular Necrosis PMID 24768677 2014 Genome-wide association study identifies variants associated with autoimmune hepatitis type 1.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Celiac Disease PMID 20190752 2010 Multiple common variants for celiac disease influencing immune gene expression.

PMID 17558408 2007 A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Colitis, Collagenous PMID 26525574 2017 Dense genotyping of immune-related loci identifies HLA variants associated with increased risk of collagenous colitis.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Diabetes Mellitus, Insulin-Dependent PMID 17632545 2007 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Diastolic blood pressure PMID 27618452 2016 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Immunoglobulin A measurement PMID 20694011 2010 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Inflammatory Bowel Diseases PMID 28008999 2016 Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Lupus Erythematosus, Cutaneous PMID 25827949 2015 Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Lupus Erythematosus, Systemic PMID 18204098 2008 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.

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

PMID 21408207 2011 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.

PMID 26316170 2016 Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Malignant neoplasm of lung PMID 19654303 2009 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.

PMID 22899653 2012 Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Membranous glomerulonephritis PMID 21323541 2011 Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 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.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Protein measurement PMID 20694011 2010 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Rheumatoid Arthritis PMID 17804836 2007 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.

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.

rs2187668 in LOC107986589;HLA-DQA2;HLA-DQA1 gene and Sarcoidosis PMID 26651848 2016 High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences.