RS137852621 SGCA

Health Risk Chr 17:50167716 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2D
Autosomal recessive limb-girdle muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2D
Autosomal recessive limb-girdle muscular dystrophy type 2D
Autosomal recessive limb-girdle muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2D
Population Frequencies
gnomAD ALL
0%
Other Variants in SGCA
rs137852622 rs28933693 rs397514451 rs137852623 rs387907298 rs371675217 rs398123098 rs200137051 rs143570936 rs757888349
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