RS193919335 POMGNT1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Muscle eye brain disease
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A3
Autosomal recessive limb-girdle muscular dystrophy
Muscle eye brain disease
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A3
Autosomal recessive limb-girdle muscular dystrophy
Other Variants in POMGNT1