RS61750168 GUCY2D
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cone-rod dystrophy 6
Leber congenital amaurosis 1
Retinal dystrophy
Leber congenital amaurosis
Night blindness
congenital stationary
type1i
Choroidal dystrophy
central areolar
1
GUCY2D-related disorder
GUCY2D-related recessive retinopathy
Cone-rod dystrophy 6
Leber congenital amaurosis 1
Retinal dystrophy
Other Variants in GUCY2D