RS119464998 FKTN

Health Risk Chr 9:105620001
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What This Variant Does
"[OMIM:?]
Associated Conditions
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A
4
Walker-Warburg congenital muscular dystrophy
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2M
Dilated cardiomyopathy 1X
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability)
type B4
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A
4
Walker-Warburg congenital muscular dystrophy
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2M
Other Variants in FKTN
rs119463990 rs587777813 rs398123555 rs119463996 rs587777748 rs119463991 rs587777814 rs119463992 rs119463993 rs119463994
Ask Dr. Hemsworth about this variant