List of variants in gene PYGL reported as likely benign by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002863.5(PYGL):c.928C>T (p.Arg310Cys)	rs35501326	0.00753
NM_002863.5(PYGL):c.1683C>T (p.Ser561=)	rs145471351	0.00262
NM_002863.5(PYGL):c.-31GCAGCCCGCCGC[1]	rs561479231
NM_002863.5(PYGL):c.1828-21G>A	rs75220125

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