RS794727804 OPA1

Health Risk Chr 3:193631621
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Autosomal dominant optic atrophy classic form
Stargardt disease
Optic atrophy
Inborn genetic diseases
Autosomal dominant optic atrophy classic form
Stargardt disease
Optic atrophy
Other Variants in OPA1
rs28939082 rs879255510 rs80356530 rs879255560 rs121908375 rs104893753 rs879255511 rs879255512 rs80356531 rs121908376
Ask Dr. Hemsworth about this variant