RS104894691 FKRP

Health Risk Chr 19:46756349
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2I
Walker-Warburg congenital muscular dystrophy
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A1
Cardiovascular phenotype
type A5
Autosomal recessive limb-girdle muscular dystrophy
Muscular dystrophy-dystroglycanopathy type B5
Autosomal recessive limb-girdle muscular dystrophy type 2I
Walker-Warburg congenital muscular dystrophy
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
type A1
Cardiovascular phenotype
type A5
Autosomal recessive limb-girdle muscular dystrophy
Other Variants in FKRP
rs104894679 rs104894680 rs104894681 rs28937900 rs587777823 rs104894682 rs28937901 rs28937902 rs28937903 rs28937904
Ask Dr. Hemsworth about this variant