RS104894149 CYP17A1

Health Risk Chr 10:102832611
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What This Variant Does
"c.1039C&gt
Associated Conditions
17-alpha-hydroxylase/17
20-lyase deficiency
combined partial
Congenital adrenal hyperplasia
Deficiency of steroid 17-alpha-monooxygenase
ADRENAL HYPERPLASIA
CONGENITAL
DUE TO 21-HYDROXYLASE DEFICIENCY
17-alpha-hydroxylase/17
20-lyase deficiency
combined partial
Congenital adrenal hyperplasia
Deficiency of steroid 17-alpha-monooxygenase
ADRENAL HYPERPLASIA
CONGENITAL
Other Variants in CYP17A1
rs556794126 rs121434319 rs1844147475 rs104894135 rs104894136 rs104894137 rs2134081192 rs104894138 rs1564777724 rs61754278
Ask Dr. Hemsworth about this variant