ClinVar Miner

List of variants in gene GYS2 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 35
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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.1553A>C (p.Glu518Ala) rs150433001 0.00173
NM_021957.4(GYS2):c.1701G>A (p.Leu567=) rs78337075 0.00092
NM_021957.4(GYS2):c.304-17T>C rs3765094 0.00067
NM_021957.4(GYS2):c.1710T>C (p.Phe570=) rs149907949 0.00056
NM_021957.4(GYS2):c.1251C>T (p.Asn417=) rs139882761 0.00031
NM_021957.4(GYS2):c.1063-15C>G rs150691568 0.00016
NM_021957.4(GYS2):c.1767T>C (p.Thr589=) rs147417298 0.00014
NM_021957.4(GYS2):c.736C>T (p.Arg246Ter) rs121918419 0.00009
NM_021957.4(GYS2):c.615C>T (p.His205=) rs569279347 0.00008
NM_021957.4(GYS2):c.750T>C (p.His250=) rs200713752 0.00005
NM_021957.4(GYS2):c.831T>C (p.Val277=) rs756223943 0.00004
NM_021957.4(GYS2):c.756T>C (p.Ala252=) rs886049159 0.00002
NM_021957.4(GYS2):c.942-7del rs537907545 0.00001
NM_021957.4(GYS2):c.1062+1G>T rs781511110
NM_021957.4(GYS2):c.1557_1579del (p.Thr520fs)
NM_021957.4(GYS2):c.1809+4_1809+13del
NM_021957.4(GYS2):c.1890+25del rs36023861
NM_021957.4(GYS2):c.789A>G (p.Ala263=) rs886038665
NM_021957.4(GYS2):c.840C>T (p.Asn280=)

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