RS775796581 CNGB3
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Abnormal electroretinogram
Nystagmus
Achromatopsia 3
Leber congenital amaurosis
Achromatopsia
Retinal dystrophy
Abnormal electroretinogram
Nystagmus
Achromatopsia 3
Leber congenital amaurosis
Achromatopsia
Retinal dystrophy
Other Variants in CNGB3