RS104894187 RGR

Health Risk Chr 10:84247706 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Retinitis pigmentosa 44
Cone dystrophy
Retinal dystrophy
Retinitis pigmentosa 44
Cone dystrophy
Retinal dystrophy
Population Frequencies
gnomAD ALL
100%
Other Variants in RGR
rs143761967 rs143720091 rs138630905 rs1554824273 rs1589337745 rs761554381 rs749839913 rs575867273 rs748553756 rs760426665
Ask Dr. Hemsworth about this variant