Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.120 GeneticVariation GWASDB GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region. 24871463

2014

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.120 GeneticVariation GWASDB Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci. 18204446

2008

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.100 GeneticVariation GWASDB Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis. 24837172

2015

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation GWASDB A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. 23760081

2013

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections
0.100 GeneticVariation GWASDB A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). 23326239

2013

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.100 GeneticVariation GWASDB Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis. 23577725

2013

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.100 GeneticVariation GWASDB Seven new loci associated with age-related macular degeneration. 23455636

2013

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.100 GeneticVariation GWASDB GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. 23263863

2013

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.100 GeneticVariation GWASDB Genome-wide association study of serum albumin:globulin ratio in Korean populations. 23303382

2013

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.100 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C2698399
Disease: Myeloperoxidase Measurement
Myeloperoxidase Measurement
0.100 GeneticVariation GWASDB Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. 23620142

2013

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271

2012

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
0.100 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.100 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.100 GeneticVariation GWASDB Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. 22899653

2012

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.100 GeneticVariation GWASDB Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes. 22705344

2012

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.100 GeneticVariation GWASDB Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3. 22694956

2012

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia
0.100 GeneticVariation GWASDB A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia. 22541561

2012

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.100 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761

2011

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.100 GeneticVariation GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946

2011

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.100 GeneticVariation GWASDB Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population. 21909106

2011

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.100 GeneticVariation GWASDB Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. 21665990

2011

Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. 20598377

2010