RS767044154 CYP11B2

Health Risk Chr 8:142917777
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Associated Conditions
Inborn genetic diseases
Corticosterone 18-monooxygenase deficiency
Corticosterone methyloxidase type 2 deficiency
Inborn genetic diseases
Corticosterone 18-monooxygenase deficiency
Corticosterone methyloxidase type 2 deficiency
Other Variants in CYP11B2
rs28931609 rs2130336602 rs72554627 rs121912977 rs121912978 rs1799998 rs72554626 rs121912979 rs104894072 rs878852988
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