ClinVar Miner

List of variants reported as likely benign for Long QT syndrome 6

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_172201.2(KCNE2):c.317C>T (p.Ser106Leu) rs183427173 0.00064
NM_172201.2(KCNE2):c.170T>C (p.Ile57Thr) rs74315448 0.00063
NM_172201.2(KCNE2):c.40G>A (p.Val14Ile) rs142153692 0.00053
NM_172201.2(KCNE2):c.29C>T (p.Thr10Met) rs199473648 0.00025
NM_172201.2(KCNE2):c.80G>A (p.Arg27His) rs148968498 0.00025
NM_172201.2(KCNE2):c.153G>T (p.Leu51=) rs143767851 0.00019
NM_172201.2(KCNE2):c.354G>A (p.Gly118=) rs187917779 0.00019
NM_172201.2(KCNE2):c.39C>T (p.Asp13=) rs556106127 0.00006
NM_172201.2(KCNE2):c.79C>T (p.Arg27Cys) rs74315449 0.00006
NM_172201.2(KCNE2):c.252C>T (p.Tyr84=) rs1028976664 0.00005
NM_172201.2(KCNE2):c.-85G>A rs41315511 0.00004
NM_172201.2(KCNE2):c.207G>A (p.Val69=) rs780534713 0.00004
NM_172201.2(KCNE2):c.222C>T (p.Ser74=) rs755211128 0.00004
NM_172201.2(KCNE2):c.228A>G (p.Arg76=) rs202169020 0.00004
NM_172201.2(KCNE2):c.309A>G (p.Leu103=) rs1387119980 0.00004
NM_172201.2(KCNE2):c.75T>C (p.Asn25=) rs372013275 0.00003
NM_172201.2(KCNE2):c.204G>A (p.Leu68=) rs200403369 0.00002
NM_172201.2(KCNE2):c.348G>A (p.Ala116=) rs16991657 0.00002
NM_172201.2(KCNE2):c.246C>T (p.Asp82=) rs774193019 0.00001
NM_172201.2(KCNE2):c.261C>T (p.Tyr87=) rs587781005 0.00001
NM_172201.2(KCNE2):c.318G>A (p.Ser106=) rs781438592 0.00001
NM_172201.2(KCNE2):c.351T>G (p.Ala117=) rs1568814278 0.00001
NM_172201.2(KCNE2):c.60T>C (p.Ile20=) rs1213881768 0.00001
NM_172201.2(KCNE2):c.*11A>C rs558860396
NM_172201.2(KCNE2):c.141C>T (p.Tyr47=)
NM_172201.2(KCNE2):c.183T>G (p.Ser61=)
NM_172201.2(KCNE2):c.195G>T (p.Val65=)
NM_172201.2(KCNE2):c.301T>C (p.Leu101=)
NM_172201.2(KCNE2):c.30G>A (p.Thr10=) rs751014874
NM_172201.2(KCNE2):c.330C>A (p.Ile110=)
NM_172201.2(KCNE2):c.339C>T (p.Asn113=) rs756380802
NM_172201.2(KCNE2):c.354G>C (p.Gly118=)
NM_172201.2(KCNE2):c.369C>T (p.Pro123=) rs2123424404
NM_172201.2(KCNE2):c.42C>A (p.Val14=) rs2123423554
NM_172201.2(KCNE2):c.87C>T (p.Asn29=) rs1427987437

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