RS397517921 SGCD

Health Risk Chr 5:156594936
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What This Variant Does
"CLNSIG=4
Associated Conditions
Neuromuscular disease
Autosomal recessive limb-girdle muscular dystrophy type 2F
Neuromuscular disease
Autosomal recessive limb-girdle muscular dystrophy type 2F
Other Variants in SGCD
rs1369919728 rs121909295 rs121909296 rs121909297 rs267607045 rs397516338 rs7717393 rs7724969 rs200670993 rs74846539
Ask Dr. Hemsworth about this variant