RS1057517051 SGCB

Health Risk Chr 4:52028799
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2E
Autosomal recessive limb-girdle muscular dystrophy type 2E
Other Variants in SGCB
rs28936383 rs104893868 rs751427729 rs1578125670 rs104893869 rs104893870 rs104893871 rs150518260 rs398123262 rs398123263
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