RS1360832162 CFAP52

Health Risk Chr 17:9633016
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Associated Conditions
Situs inversus
Oculomotor apraxia
Heterotaxy
visceral
10
autosomal
with male infertility
Situs inversus
Oculomotor apraxia
Heterotaxy
visceral
10
autosomal
with male infertility
Other Variants in CFAP52
rs139646620 rs146845939 rs141646758 rs746987839 rs752819814 rs775639416
Ask Dr. Hemsworth about this variant