ClinVar Miner

List of variants in gene KCNQ1 reported as uncertain significance for Arrhythmia

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Total variants: 21
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HGVS dbSNP
NM_181798.1(KCNQ1):c.1007G>C (p.Ser336Thr) rs184636161
NM_181798.1(KCNQ1):c.1174C>T (p.Arg392Cys) rs199472787
NM_181798.1(KCNQ1):c.1240G>A (p.Val414Ile) rs199472796
NM_181798.1(KCNQ1):c.1339A>G (p.Ile447Val) rs761947465
NM_181798.1(KCNQ1):c.160C>T (p.Arg54Cys) rs199473395
NM_181798.1(KCNQ1):c.1630G>A (p.Gly544Ser) rs764563996
NM_181798.1(KCNQ1):c.203G>A (p.Arg68Gln) rs138362632
NM_181798.1(KCNQ1):c.415C>A (p.Leu139Met) rs1263583359
NM_181798.1(KCNQ1):c.439A>G (p.Ile147Val) rs199472728
NM_181798.1(KCNQ1):c.479C>A (p.Ala160Glu) rs199472735
NM_181798.1(KCNQ1):c.499G>A (p.Val167Met) rs749073770
NM_181798.1(KCNQ1):c.728C>T (p.Ala243Val) rs775362401
NM_181798.1(KCNQ1):c.77C>T (p.Thr26Met) rs143709408
NM_181798.1(KCNQ1):c.808C>T (p.Arg270Trp) rs199472776
NM_181798.1(KCNQ1):c.815C>G (p.Ala272Gly) rs876657836
NM_181798.1(KCNQ1):c.875A>G (p.Lys292Arg) rs757328965
NM_181798.1(KCNQ1):c.968A>G (p.Glu323Gly) rs1057518902
NM_181798.1(KCNQ1):c.971G>A (p.Arg324Gln) rs199472781
NM_181798.1(KCNQ1):c.974G>A (p.Arg325Gln) rs145229963
NM_181798.1(KCNQ1):c.994G>A (p.Asp332Asn) rs747704276
NM_181798.1(KCNQ1):c.997G>A (p.Gly333Ser) rs199472783

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