RS104894138 CYP17A1
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What This Variant Does
"c.286C>
Associated Conditions
17-alpha-hydroxylase/17
20-lyase deficiency
combined complete
Deficiency of steroid 17-alpha-monooxygenase
Congenital adrenal hyperplasia
Differences in sex development
17-alpha-hydroxylase/17
20-lyase deficiency
combined complete
Deficiency of steroid 17-alpha-monooxygenase
Congenital adrenal hyperplasia
Differences in sex development
Other Variants in CYP17A1