RS104893612 CNGA3

Health Risk Chr 2:98389696
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What This Variant Does
"[OMIM:?]
Associated Conditions
Achromatopsia 2
Retinal dystrophy
Achromatopsia
Inborn genetic diseases
Achromatopsia 2
Retinal dystrophy
Achromatopsia
Inborn genetic diseases
Other Variants in CNGA3
rs104893613 rs104893614 rs104893615 rs104893616 rs104893617 rs137852608 rs104893619 rs104893620 rs104893621 rs141086649
Ask Dr. Hemsworth about this variant