RS6447 CYP21A2
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Associated Conditions
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
CYP21A2-related disorder
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
CYP21A2-related disorder
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Serum levels of protein C4A;C4B | A | OR: 0.68 | 1E-18 | PubMed |
Other Variants in CYP21A2