RS119463992 FKTN
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2M
Walker-Warburg congenital muscular dystrophy
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A
4
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability)
type B4
Dilated cardiomyopathy 1X
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2M
Walker-Warburg congenital muscular dystrophy
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A
4
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability)
Other Variants in FKTN