RS61755814 PRPH2

Health Risk Chr 6:42704478
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What This Variant Does
"CLNSIG=5
Associated Conditions
Macular dystrophy
Stargardt disease
PRPH2-related disorder
Patterned dystrophy of the retinal pigment epithelium
Choroidal dystrophy
central areolar 2
Retinal dystrophy
Macular dystrophy
Stargardt disease
PRPH2-related disorder
Patterned dystrophy of the retinal pigment epithelium
Choroidal dystrophy
central areolar 2
Retinal dystrophy
Other Variants in PRPH2
rs61755777 rs61755806 rs121918563 rs61755793 rs121918564 rs61755789 rs61755792 rs61748429 rs61755816 rs61755798
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