RS61755802 PRPH2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Leber congenital amaurosis 18
Patterned macular dystrophy 1
PRPH2-related disorder
PRPH2-related disorder
PRPH2-related disorder
Leber congenital amaurosis 18
Patterned macular dystrophy 1
PRPH2-related disorder
PRPH2-related disorder
PRPH2-related disorder
Other Variants in PRPH2