RS104894143 CYP17A1
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What This Variant Does
"[OMIM:?]
Associated Conditions
17-alpha-hydroxylase/17
20-lyase deficiency
combined complete
Deficiency of steroid 17-alpha-monooxygenase
17-alpha-hydroxylase/17
20-lyase deficiency
combined complete
Deficiency of steroid 17-alpha-monooxygenase
Other Variants in CYP17A1