RS761628767 NR2E3

Health Risk Chr 15:71813567
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Retinitis pigmentosa 37
Enhanced S-cone syndrome
Retinitis pigmentosa 37
Enhanced S-cone syndrome
Other Variants in NR2E3
rs104894492 rs104894493 rs1567159701 rs28937873 rs121912631 rs1567160967 rs527236086 rs730882149 rs2723341 rs786205493
Ask Dr. Hemsworth about this variant