RS372556807 CYP11B2
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Associated Conditions
Corticosterone methyloxidase type 2 deficiency
Corticosterone 18-monooxygenase deficiency
Glucocorticoid-remediable aldosteronism
Inborn genetic diseases
Hypoaldosteronism
congenital
Corticosterone methyloxidase type 2 deficiency
Corticosterone 18-monooxygenase deficiency
Glucocorticoid-remediable aldosteronism
Inborn genetic diseases
Hypoaldosteronism
congenital
Other Variants in CYP11B2