RS121909297 SGCD
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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 type 2F
Dilated cardiomyopathy 1L
Other Variants in SGCD