RS774216266 NR5A1

Health Risk Chr 9:124500367
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Associated Conditions
46
XY disorder of sex development
Oligosynaptic infertility
Male infertility with azoospermia or oligozoospermia due to single gene mutation
46
XY disorder of sex development
Oligosynaptic infertility
Male infertility with azoospermia or oligozoospermia due to single gene mutation
Other Variants in NR5A1
rs121918654 rs104894119 rs2538674111 rs104894123 rs606231205 rs104894124 rs104894125 rs104894126 rs104894120 rs606231206
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