RS28931609 CYP11B2
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What This Variant Does
"[OMIM:CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY]
Associated Conditions
Corticosterone methyl oxidase type II deficiency
Early-onset familial hypoaldosteronism
Corticosterone 18-monooxygenase deficiency
Corticosterone methyloxidase type 2 deficiency
Corticosterone methyl oxidase type II deficiency
Early-onset familial hypoaldosteronism
Corticosterone 18-monooxygenase deficiency
Corticosterone methyloxidase type 2 deficiency
Other Variants in CYP11B2