RS139701867 POMGNT1
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2O
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability)
type B3
Retinitis pigmentosa 76
Muscle eye brain disease
Inborn genetic diseases
Autosomal recessive limb-girdle muscular dystrophy type 2O
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability)
type B3
Retinitis pigmentosa 76
Muscle eye brain disease
Inborn genetic diseases
Other Variants in POMGNT1