|
| 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
|
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
|
Rheumatoid Arthritis
|
0.100 |
GeneticVariation |
GWASDB |
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.
|
17804836 |
2007 |
|
| Entrez Id: |
1589 |
| Gene Symbol: |
CYP21A2 |
CYP21A2
|
Rheumatoid Arthritis
|
0.100 |
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 |
|
| 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
|
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
|
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
|
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
|
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
|
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
|
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
|
Multiple Sclerosis
|
0.100 |
GeneticVariation |
GWASDB |
Risk alleles for multiple sclerosis identified by a genomewide study.
|
17660530 |
2007 |
|
| 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
|
Systemic Scleroderma
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
|
20383147 |
2010 |
|
| 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
|
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
|
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
|
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
|
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
|
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 |
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 |