RS527236092 PRCD

Health Risk Chr 17:76540143
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Retinitis pigmentosa
Retinitis pigmentosa 36
Retinal dystrophy
Retinitis pigmentosa
Retinitis pigmentosa 36
Retinal dystrophy
Other Variants in PRCD
rs387907268 rs2074970792 rs773201535 rs2074979029 rs200645008 rs757471313 rs527451635 rs779066277 rs1009828411 rs2143140372
Ask Dr. Hemsworth about this variant