RS119463996 FKTN
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2M
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A1
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability)
type B4
Autosomal recessive limb-girdle muscular dystrophy type 2M
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A1
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability)
type B4
Other Variants in FKTN