RS141656719 CAPN3
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2A
Muscular dystrophy
limb-girdle
autosomal dominant 4
CAPN3-related disorder
Autosomal recessive limb-girdle muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2A
Muscular dystrophy
limb-girdle
autosomal dominant 4
CAPN3-related disorder
Autosomal recessive limb-girdle muscular dystrophy
Other Variants in CAPN3