RS192003551 RPGRIP1

Health Risk Chr 14:21294745
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Cone-rod dystrophy 13
Leber congenital amaurosis 6
Retinitis pigmentosa
Cone-rod dystrophy 13
Leber congenital amaurosis 6
Retinitis pigmentosa
Other Variants in RPGRIP1
rs137853124 rs28937883 rs181758389 rs398124354 rs398124355 rs398124356 rs61751266 rs61751268 rs61751271 rs61751265
Ask Dr. Hemsworth about this variant