RS104894681 FKRP

Health Risk Chr 19:46756793
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What This Variant Does
"[OMIM:?]
Associated Conditions
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A5
type A1
Autosomal recessive limb-girdle muscular dystrophy type 2I
Muscular dystrophy-dystroglycanopathy type B5
Muscular dystrophy-dystroglycanopathy (congenital without impaired intellectual development)
type B
5
Cardiovascular phenotype
Walker-Warburg congenital muscular dystrophy
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A5
type A1
Autosomal recessive limb-girdle muscular dystrophy type 2I
Muscular dystrophy-dystroglycanopathy type B5
Other Variants in FKRP
rs104894679 rs104894680 rs28937900 rs587777823 rs104894682 rs28937901 rs28937902 rs28937903 rs28937904 rs28937905
Ask Dr. Hemsworth about this variant