List of variants in gene GYS2 reported as benign by Illumina Laboratory Services, Illumina

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: 15

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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.*152C>T	rs936	0.46898
NM_021957.4(GYS2):c.*6A>T	rs10431213	0.30676
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.1245C>G (p.Asp415Glu)	rs16924002	0.02117
NM_021957.4(GYS2):c.1965G>C (p.Gln655His)	rs117639846	0.02061
NM_021957.4(GYS2):c.1636A>G (p.Thr546Ala)	rs61733199	0.01511
NM_021957.4(GYS2):c.280G>A (p.Ala94Thr)	rs34225615	0.00845
NM_021957.4(GYS2):c.1872A>G (p.Glu624=)	rs142883971	0.00562
NM_021957.4(GYS2):c.577G>A (p.Ala193Thr)	rs16924038	0.00462
NM_021957.4(GYS2):c.2005G>A (p.Asp669Asn)	rs142656537	0.00146
NM_021957.4(GYS2):c.*290G>T	rs17849015

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