RS878853383 CRX
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Retinal dystrophy
Leber congenital amaurosis 7
Cone-rod dystrophy 2
Retinal dystrophy
Leber congenital amaurosis 7
Cone-rod dystrophy 2
Other Variants in CRX