RS143962150 SGCA

Health Risk Chr 17:50168506
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2D
Autosomal recessive limb-girdle muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2D
Other Variants in SGCA
rs137852621 rs137852622 rs28933693 rs397514451 rs137852623 rs387907298 rs371675217 rs398123098 rs200137051 rs143570936
Ask Dr. Hemsworth about this variant