RS796065331 RPGR

Health Risk Chr X:38310737
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
RPGR-related retinopathy
Retinal dystrophy
RPGR-related retinopathy
Retinal dystrophy
Other Variants in RPGR
rs62638651 rs62642057 rs62638634 rs62638637 rs137852549 rs606231180 rs606231181 rs62638646 rs2147248070 rs137852550
Ask Dr. Hemsworth about this variant