RS2723341 NR2E3
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What This Variant Does
"CLNSIG=255
Associated Conditions
Enhanced S-cone syndrome
Retinitis pigmentosa 37
NR2E3-related disorder
Retinal dystrophy
Color vision defect
Horizontal nystagmus
Visual impairment
Cone-rod dystrophy
Retinitis pigmentosa
Goldmann-Favre syndrome
Ocular albinism
Inborn genetic diseases
Enhanced S-cone syndrome
Enhanced S-cone syndrome
Retinitis pigmentosa 37
Other Variants in NR2E3