RS104894683 FKRP

Health Risk Chr 19:46755685
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2I
Walker-Warburg congenital muscular dystrophy
Cardiovascular phenotype
Autosomal recessive limb-girdle muscular dystrophy type 2I
Walker-Warburg congenital muscular dystrophy
Cardiovascular phenotype
Other Variants in FKRP
rs104894679 rs104894680 rs104894681 rs28937900 rs587777823 rs104894682 rs28937901 rs28937902 rs28937903 rs28937904
Ask Dr. Hemsworth about this variant