RS137853137 CRB1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Retinitis pigmentosa 12
Leber congenital amaurosis 8
Retinal dystrophy
Retinitis pigmentosa
Leber congenital amaurosis
Pigmented paravenous retinochoroidal atrophy
CRB1-related disorder
Retinitis pigmentosa 12
Leber congenital amaurosis 8
Retinal dystrophy
Retinitis pigmentosa
Leber congenital amaurosis
Pigmented paravenous retinochoroidal atrophy
CRB1-related disorder
Other Variants in CRB1