RS11903223 DYSF
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What This Variant Does
"A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in ...
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2B
Neuromuscular disease caused by qualitative or quantitative defects of dysferlin
Autosomal recessive limb-girdle muscular dystrophy type 2B
Neuromuscular disease caused by qualitative or quantitative defects of dysferlin
Other Variants in DYSF