RS192619553 CFAP53

Health Risk Chr 18:50227413
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Associated Conditions
Heterotaxy
visceral
6
autosomal
Inborn genetic diseases
Heterotaxy
visceral
6
autosomal
Inborn genetic diseases
Other Variants in CFAP53
rs2144412496 rs375801610 rs1555672928 rs369539291 rs897584290 rs778118886 rs557771609 rs377709493 rs1178515683
Ask Dr. Hemsworth about this variant