RS116987552 PYGM
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What This Variant Does
"aka c.148C>
Associated Conditions
Glycogen storage disease
type V
Inborn genetic diseases
See cases
Tip-toe gait
Hereditary skeletal muscle disorder
Glycogen storage disease
type V
Inborn genetic diseases
See cases
Tip-toe gait
Hereditary skeletal muscle disorder
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Urate levels | A | OR: 0.15 | 2E-16 | PubMed |
Other Variants in PYGM