RS104894072 CYP11B2

Health Risk Chr 8:142915046 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Corticosterone 18-monooxygenase deficiency
Corticosterone methyloxidase type 2 deficiency
Corticosterone 18-monooxygenase deficiency
Corticosterone methyloxidase type 2 deficiency
Population Frequencies
gnomAD ALL
100%
Other Variants in CYP11B2
rs28931609 rs2130336602 rs72554627 rs121912977 rs121912978 rs1799998 rs72554626 rs121912979 rs878852988 rs375938097
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