RS200137051 SGCA

Health Risk Chr 17:50167962
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Associated Conditions
Sarcoglycanopathy
Hypertrophic cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2D
SGCA-related disorder
Inborn genetic diseases
Sarcoglycanopathy
Hypertrophic cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2D
SGCA-related disorder
Inborn genetic diseases
Other Variants in SGCA
rs137852621 rs137852622 rs28933693 rs397514451 rs137852623 rs387907298 rs371675217 rs398123098 rs143570936 rs757888349
Ask Dr. Hemsworth about this variant