RS138642840 POMGNT1
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What This Variant Does
"CLNSIG=255
Associated Conditions
Muscle eye brain disease
POMGNT1-related disorder
Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies
Autosomal recessive limb-girdle muscular dystrophy type 2O
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability)
type B3
Retinitis pigmentosa 76
Autosomal recessive limb-girdle muscular dystrophy
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A3
Muscular dystrophy-dystroglycanopathy
Myopathy caused by variation in POMGNT1
Retinal dystrophy
Cervical cancer
Malignant tumor of esophagus
Other Variants in POMGNT1