RS540215492 GYS2

Health Risk Chr 12:21540529
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Glycogen storage disorder due to hepatic glycogen synthase deficiency
Inborn genetic diseases
Glycogen storage disorder due to hepatic glycogen synthase deficiency
Other Variants in GYS2
rs121918419 rs587776831 rs121918420 rs121918421 rs121918422 rs121918423 rs121918424 rs267603422 rs186184722 rs150433001
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