RS794727392 OPA1

Health Risk Chr 3:193662963
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What This Variant Does
"CLNSIG=5
Associated Conditions
OPA1-related disorder
Inborn genetic diseases
Optic atrophy
OPA1-related disorder
Inborn genetic diseases
Optic atrophy
Other Variants in OPA1
rs28939082 rs879255510 rs80356530 rs879255560 rs121908375 rs104893753 rs879255511 rs879255512 rs80356531 rs121908376
Ask Dr. Hemsworth about this variant