RS61755765 PRPH2

Health Risk Chr 6:42722261
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Associated Conditions
Retinitis punctata albescens
autosomal dominant
Retinitis punctata albescens
autosomal dominant
Other Variants in PRPH2
rs61755777 rs61755806 rs121918563 rs61755793 rs121918564 rs61755789 rs61755792 rs61748429 rs61755816 rs61755798
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