RS113993981 PYGL

Health Risk Chr 14:50913028
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What This Variant Does
"Identification of a mutation in liver glycogen phosphorylase in glycogen storage disease type VI. [...
Associated Conditions
Glycogen storage disease
type VI
Thyroid cancer
nonmedullary
1
Acute myeloid leukemia
Glycogen storage disease
type VI
Glycogen storage disease
type VI
Glycogen storage disease
type VI
Thyroid cancer
nonmedullary
1
Other Variants in PYGL
rs113993982 rs113993974 rs113993977 rs113993978 rs113993979 rs113993980 rs35026927 rs113993986 rs113993973 rs113993975
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