ClinVar Miner

List of variants in gene GYS2 reported as benign for not specified

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Gene type:
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Total variants: 19
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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.1229+40T>C rs1871136 0.74383
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.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.1423-21A>G rs73238708 0.01308
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.2054T>C (p.Phe685Ser) rs117474773 0.00404
NM_021957.4(GYS2):c.421G>A (p.Gly141Ser) rs149533049 0.00192
NM_021957.4(GYS2):c.2005G>A (p.Asp669Asn) rs142656537 0.00146
NM_021957.4(GYS2):c.304-17T>C rs3765094 0.00067

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