RS61755781 PRPH2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Patterned macular dystrophy 1
PRPH2-related disorder
Retinal dystrophy
Cone-rod dystrophy
Stargardt disease
Autosomal recessive bestrophinopathy
Patterned dystrophy of the retinal pigment epithelium
Retinitis pigmentosa
Vitelliform macular dystrophy 3
Choroidal dystrophy
central areolar 2
Retinitis pigmentosa 7
Pigmentary retinal dystrophy
Patterned macular dystrophy 1
PRPH2-related disorder
Other Variants in PRPH2