RS144099488 CNGA3

Health Risk Chr 2:98383432
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Associated Conditions
Achromatopsia 2
Inborn genetic diseases
Retinal dystrophy
Achromatopsia 2
Inborn genetic diseases
Retinal dystrophy
Other Variants in CNGA3
rs104893612 rs104893613 rs104893614 rs104893615 rs104893616 rs104893617 rs137852608 rs104893619 rs104893620 rs104893621
Ask Dr. Hemsworth about this variant