RS119463995 FKTN

Health Risk Chr 9:105601319
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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 A
4
Walker-Warburg congenital muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2M
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A
4
Walker-Warburg congenital muscular dystrophy
Other Variants in FKTN
rs119463990 rs587777813 rs398123555 rs119463996 rs587777748 rs119463991 rs587777814 rs119463992 rs119463993 rs119463994
Ask Dr. Hemsworth about this variant