RS398123802 DYSF
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2B
Neuromuscular disease caused by qualitative or quantitative defects of dysferlin
Abnormality of the musculature
Autosomal recessive limb-girdle muscular dystrophy
Miyoshi muscular dystrophy 1
Autosomal recessive limb-girdle muscular dystrophy type 2B
Neuromuscular disease caused by qualitative or quantitative defects of dysferlin
Abnormality of the musculature
Autosomal recessive limb-girdle muscular dystrophy
Miyoshi muscular dystrophy 1
Other Variants in DYSF