RS104893620 CNGA3

Health Risk Chr 2:98395999
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What This Variant Does
"[OMIM:?]
Associated Conditions
Achromatopsia 2
Achromatopsia
Color vision defect
Macular degeneration
Photophobia
Retinal dystrophy
Optic atrophy
Achromatopsia 2
Achromatopsia
Color vision defect
Macular degeneration
Photophobia
Retinal dystrophy
Optic atrophy
Other Variants in CNGA3
rs104893612 rs104893613 rs104893614 rs104893615 rs104893616 rs104893617 rs137852608 rs104893619 rs104893621 rs141086649
Ask Dr. Hemsworth about this variant