RS113993982 PYGL

Health Risk Chr 14:50912155
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What This Variant Does
"Mutations in the liver glycogen phosphorylase gene (PYGL) underlying glycogenosis type VI. [OMIM:?]
Associated Conditions
Glycogen storage disease
type VI
Uterine corpus endometrial carcinoma
Uveal melanoma
Glycogen storage disease
type VI
Uterine corpus endometrial carcinoma
Uveal melanoma
Other Variants in PYGL
rs113993974 rs113993977 rs113993981 rs113993978 rs113993979 rs113993980 rs35026927 rs113993986 rs113993973 rs113993975
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