RS121918419 GYS2

Health Risk Chr 12:21568952
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What This Variant Does
"rs121918419, also known as c.736C&gt
Associated Conditions
Glycogen storage disorder due to hepatic glycogen synthase deficiency
Glycogen storage disease
See cases
GYS2-related disorder
Thymoma
Glycogen storage disorder due to hepatic glycogen synthase deficiency
Glycogen storage disease
See cases
GYS2-related disorder
Thymoma
Other Variants in GYS2
rs587776831 rs121918420 rs121918421 rs121918422 rs121918423 rs121918424 rs267603422 rs540215492 rs186184722 rs150433001
Ask Dr. Hemsworth about this variant