RS398123262 SGCB

Health Risk Chr 4:52038259
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2E
Primary dilated cardiomyopathy
Abnormality of the musculature
Autosomal recessive limb-girdle muscular dystrophy type 2E
Primary dilated cardiomyopathy
Abnormality of the musculature
Other Variants in SGCB
rs28936383 rs104893868 rs751427729 rs1578125670 rs104893869 rs104893870 rs104893871 rs150518260 rs398123263 rs796065319
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