RS121908110 FKRP
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What This Variant Does
"[OMIM:?]
Associated Conditions
Muscular dystrophy
Walker-Warburg congenital muscular dystrophy
Muscular dystrophy-dystroglycanopathy type B5
Autosomal recessive limb-girdle muscular dystrophy type 2I
Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development)
type B
5
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A1
type A5
Autosomal recessive limb-girdle muscular dystrophy
Cardiovascular phenotype
Muscular dystrophy
Walker-Warburg congenital muscular dystrophy
Muscular dystrophy-dystroglycanopathy type B5
Other Variants in FKRP