RS758281815 CYP11B2

Health Risk Chr 8:142914416
Upload your DNA to see your genotype for this variant.
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
Ask Dr. Hemsworth about this variant