List of variants in gene PYGM reported as 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005609.4(PYGM):c.1827+7A>G	rs532747	0.10554
NM_005609.4(PYGM):c.1494C>T (p.Pro498=)	rs11231865	0.03355
NM_005609.4(PYGM):c.425-22C>T	rs61884454	0.02517
NM_005609.4(PYGM):c.1184C>T (p.Thr395Met)	rs71581787	0.01778
NM_005609.4(PYGM):c.1240C>G (p.Arg414Gly)	rs11231866

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