Entrez Id: |
1589 |
Gene Symbol: |
CYP21A2 |
CYP21A2
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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 |
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 |