RS28937900 FKRP
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What This Variant Does
"rs28937900, also known as c.826C>
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2I
Walker-Warburg congenital muscular dystrophy
Muscular dystrophy-dystroglycanopathy
Limb-girdle muscular dystrophy
Muscular dystrophy-dystroglycanopathy type B5
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A5
8 conditions
Myopathy
Autosomal recessive limb-girdle muscular dystrophy
Cardiovascular phenotype
Myopathy caused by variation in FKRP
FKRP-related disorder
Neuronopathy
distal hereditary motor
Other Variants in FKRP