RS527236098 PRPH2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Retinitis pigmentosa
PRPH2-related disorder
Retinal dystrophy
Stargardt disease
Retinitis pigmentosa
PRPH2-related disorder
Retinal dystrophy
Stargardt disease
Other Variants in PRPH2