Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
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
|
Diabetes Mellitus, Insulin-Dependent
|
0.100 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.
|
17632545 |
2007 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
Adenocarcinoma of lung (disorder)
|
0.100 |
GeneticVariation |
GWASDB |
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
|
19836008 |
2009 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
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
|
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
|
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
|
Malignant neoplasm of lung
|
0.100 |
GeneticVariation |
GWASDB |
Common 5p15.33 and 6p21.33 variants influence lung cancer risk.
|
18978787 |
2008 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
|
0.100 |
GeneticVariation |
GWASDB |
Common genetic variation and the control of HIV-1 in humans.
|
20041166 |
2009 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
HIV-1, RESISTANCE TO
|
0.100 |
GeneticVariation |
GWASDB |
Common genetic variation and the control of HIV-1 in humans.
|
20041166 |
2009 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
|
0.100 |
GeneticVariation |
GWASDB |
Common genetic variation and the control of HIV-1 in humans.
|
20041166 |
2009 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
AIDS, PROGRESSION TO
|
0.100 |
GeneticVariation |
GWASDB |
Common genetic variation and the control of HIV-1 in humans.
|
20041166 |
2009 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
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
|
Multiple Sclerosis
|
0.100 |
GeneticVariation |
GWASDB |
Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.
|
20598377 |
2010 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
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
|
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
|
Age related macular degeneration
|
0.100 |
GeneticVariation |
GWASDB |
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.
|
20385819 |
2010 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
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
|
Age related macular degeneration
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.
|
20861866 |
2010 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
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
|
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
|
Vitiligo
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC.
|
20526339 |
2010 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
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
|
Age related macular degeneration
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).
|
20385826 |
2010 |
Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
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
|
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 |