RS1057517982 PRPF31

Health Risk Chr 19:54123561
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Retinal dystrophy
See cases
Retinal dystrophy
See cases
Other Variants in PRPF31
rs587776589 rs119475042 rs587776590 rs119475043 rs1600344451 rs1600337143 rs587776591 rs144738703 rs527236094 rs527236095
Ask Dr. Hemsworth about this variant