Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9257809
rs9257809
OR5V1 ; OR12D3
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		A 0.820 GeneticVariation GWASDB Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. 22961001

2012
dbSNP: rs3094548
rs3094548
OR5V1 ; OR12D3
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		G 0.700 GeneticVariation GWASDB Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. 21946350

2011
dbSNP: rs3094548
rs3094548
OR5V1 ; OR12D3
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		G 0.700 GeneticVariation GWASDB Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. 21946350

2011
dbSNP: rs3117440
rs3117440
OR5V1 ; OR12D3
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs3749971
rs3749971
OR5V1 ; OR12D3
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		A 0.700 GeneticVariation GWASDB GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region. 24871463

2014
dbSNP: rs3749971
rs3749971
OR5V1 ; OR12D3
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.700 GeneticVariation GWASDB Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. 22899653

2012
dbSNP: rs3749971
rs3749971
OR5V1 ; OR12D3
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		0.700 GeneticVariation GWASDB Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). 19115949

2009
dbSNP: rs7753474
rs7753474
OR5V1 ; OR12D3
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088

2009
dbSNP: rs9257809
rs9257809
OR5V1 ; OR12D3
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		A 0.700 GeneticVariation GWASDB FTO genotype is associated with phenotypic variability of body mass index. 22982992

2012
dbSNP: rs9257809
rs9257809
OR5V1 ; OR12D3
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		A 0.700 GeneticVariation GWASDB FTO genotype is associated with phenotypic variability of body mass index. 22982992

2012
dbSNP: rs9257809
rs9257809
OR5V1 ; OR12D3
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007