RS6161 CYP11A1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Congenital adrenal insufficiency with 46
XY sex reversal OR 46
XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
CYP11A1-related disorder
Congenital adrenal hyperplasia
Congenital adrenal insufficiency with 46
XY sex reversal OR 46
XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
CYP11A1-related disorder
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Height | T | β: 0.05 | 1E-20 | PubMed |
Other Variants in CYP11A1