RS141647790 PDE6B
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Associated Conditions
Congenital stationary night blindness autosomal dominant 2
Retinitis pigmentosa
Inborn genetic diseases
PDE6B-related disorder
Congenital stationary night blindness autosomal dominant 2
Retinitis pigmentosa
Inborn genetic diseases
PDE6B-related disorder
Other Variants in PDE6B