RS104894137 CYP17A1

Health Risk Chr 10:102832626
Upload your DNA to see your genotype for this variant.
What This Variant Does
"c.1024C&gt
Associated Conditions
17-alpha-hydroxylase/17
20-lyase deficiency
combined partial
Deficiency of steroid 17-alpha-monooxygenase
17-alpha-hydroxylase/17
20-lyase deficiency
combined partial
Deficiency of steroid 17-alpha-monooxygenase
Other Variants in CYP17A1
rs556794126 rs121434319 rs1844147475 rs104894135 rs104894136 rs2134081192 rs104894138 rs1564777724 rs61754278 rs104894139
Ask Dr. Hemsworth about this variant