RS587777821 POMGNT1

Health Risk Chr 1:46192307
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2O
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability)
type B3
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A3
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A3
Muscular dystrophy-dystroglycanopathy
Autosomal recessive limb-girdle muscular dystrophy type 2O
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability)
type B3
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A3
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A3
Other Variants in POMGNT1
rs193919335 rs386834017 rs28942068 rs28940869 rs193919336 rs193919337 rs587777822 rs267606961 rs74374973 rs267606962
Ask Dr. Hemsworth about this variant