RS147876778 CNGB3
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Achromatopsia 3
Abnormality of the eye
Retinitis pigmentosa
Achromatopsia
Severe early-childhood-onset retinal dystrophy
Retinal dystrophy
Achromatopsia 3
Abnormality of the eye
Retinitis pigmentosa
Achromatopsia
Severe early-childhood-onset retinal dystrophy
Retinal dystrophy
Other Variants in CNGB3