RS61755776 PRPH2

Health Risk Chr 6:42722032
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Retinitis pigmentosa
PRPH2-related disorder
Retinitis pigmentosa
PRPH2-related disorder
Other Variants in PRPH2
rs61755777 rs61755806 rs121918563 rs61755793 rs121918564 rs61755789 rs61755792 rs61748429 rs61755816 rs61755798
Ask Dr. Hemsworth about this variant