RS62635654 CRB1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Retinitis pigmentosa 12
Macular dystrophy
Retinitis pigmentosa
Leber congenital amaurosis 8
CRB1-related maculopathy
Retinal dystrophy
Pigmented paravenous retinochoroidal atrophy
Retinitis pigmentosa-deafness syndrome
CRB1-related disorder
Cone-rod dystrophy
Retinitis pigmentosa 12
Macular dystrophy
Retinitis pigmentosa
Leber congenital amaurosis 8
CRB1-related maculopathy
Other Variants in CRB1