List of variants reported as benign for Glycogen storage disease due to hepatic glycogen synthase deficiency by Illumina Clinical Services Laboratory,Illumina

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Total variants: 16

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HGVS	dbSNP
NM_021957.4(GYS2):c.*152C>T	rs936
NM_021957.4(GYS2):c.*290G>T	rs0
NM_021957.4(GYS2):c.*6A>T	rs10431213
NM_021957.4(GYS2):c.1087A>G (p.Met363Val)	rs2306180
NM_021957.4(GYS2):c.1169+12A>T	rs4639981
NM_021957.4(GYS2):c.1229+11G>A	rs1871137
NM_021957.4(GYS2):c.1245C>G (p.Asp415Glu)	rs16924002
NM_021957.4(GYS2):c.1389T>C (p.Ile463=)	rs146434233
NM_021957.4(GYS2):c.1464A>G (p.Leu488=)	rs35403985
NM_021957.4(GYS2):c.1636A>G (p.Thr546Ala)	rs61733199
NM_021957.4(GYS2):c.1872A>G (p.Glu624=)	rs142883971
NM_021957.4(GYS2):c.1965G>C (p.Gln655His)	rs117639846
NM_021957.4(GYS2):c.2005G>A (p.Asp669Asn)	rs142656537
NM_021957.4(GYS2):c.2067C>T (p.His689=)	rs7954038
NM_021957.4(GYS2):c.280G>A (p.Ala94Thr)	rs34225615
NM_021957.4(GYS2):c.577G>A (p.Ala193Thr)	rs16924038

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