RS150518260 SGCB

Health Risk Chr 4:52029766
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2E
Qualitative or quantitative defects of beta-sarcoglycan
Inborn genetic diseases
Limb-girdle muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2E
Qualitative or quantitative defects of beta-sarcoglycan
Inborn genetic diseases
Limb-girdle muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy
Other Variants in SGCB
rs28936383 rs104893868 rs751427729 rs1578125670 rs104893869 rs104893870 rs104893871 rs398123262 rs398123263 rs796065319
Ask Dr. Hemsworth about this variant