RS863224958 CAPN3
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2A
Abnormality of the musculature
Autosomal recessive limb-girdle muscular dystrophy
Muscular dystrophy
limb-girdle
autosomal dominant 4
Autosomal recessive limb-girdle muscular dystrophy type 2A
Abnormality of the musculature
Autosomal recessive limb-girdle muscular dystrophy
Muscular dystrophy
limb-girdle
autosomal dominant 4
Other Variants in CAPN3