RS768588675 POMGNT1

Health Risk Chr 1:46193588
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Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2O
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability)
type B3
Retinal dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2O
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability)
type B3
Retinal dystrophy
Other Variants in POMGNT1
rs587777821 rs193919335 rs386834017 rs28942068 rs28940869 rs193919336 rs193919337 rs587777822 rs267606961 rs74374973
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