RS62645748 CRB1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Leber congenital amaurosis 8
Retinitis pigmentosa 12
Retinal dystrophy
Pigmented paravenous retinochoroidal atrophy
Retinitis pigmentosa
Leber congenital amaurosis
CRB1-related disorder
Cone dystrophy
Hereditary macular dystrophy
Leber congenital amaurosis 8
Retinitis pigmentosa 12
Retinal dystrophy
Pigmented paravenous retinochoroidal atrophy
Retinitis pigmentosa
Leber congenital amaurosis
Other Variants in CRB1