RS121909295 SGCD

Health Risk Chr 5:156595042
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2F
Dilated cardiomyopathy 1L
Autosomal recessive limb-girdle muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2F
Dilated cardiomyopathy 1L
Autosomal recessive limb-girdle muscular dystrophy
Other Variants in SGCD
rs1369919728 rs121909296 rs121909297 rs267607045 rs397516338 rs7717393 rs7724969 rs200670993 rs74846539 rs397517921
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