List of variants in gene GYS2 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_021957.4(GYS2):c.1169+12A>T	rs4639981	0.76485
NM_021957.4(GYS2):c.1229+11G>A	rs1871137	0.75356
NM_021957.4(GYS2):c.1087A>G (p.Met363Val)	rs2306180	0.74398
NM_021957.4(GYS2):c.*6A>T	rs10431213	0.30676
NM_021957.4(GYS2):c.942-17G>A	rs8192697	0.18537
NM_021957.4(GYS2):c.2067C>T (p.His689=)	rs7954038	0.02548
NM_021957.4(GYS2):c.1464A>G (p.Leu488=)	rs35403985	0.02543
NM_021957.4(GYS2):c.1965G>C (p.Gln655His)	rs117639846	0.02061
NM_021957.4(GYS2):c.1636A>G (p.Thr546Ala)	rs61733199	0.01511

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