RS786205579 PRPH2

Health Risk Chr 6:42721838
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Retinal dystrophy
PRPH2-related disorder
Retinal dystrophy
PRPH2-related disorder
Other Variants in PRPH2
rs61755777 rs61755806 rs121918563 rs61755793 rs121918564 rs61755789 rs61755792 rs61748429 rs61755816 rs61755798
Ask Dr. Hemsworth about this variant