ClinVar Miner

List of variants in gene KCNQ1 reported as likely benign for Cardiovascular phenotype

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Total variants: 23
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HGVS dbSNP
NM_000218.2(KCNQ1):c.207G>T (p.Ala69=) rs587781009
NM_000218.2(KCNQ1):c.225T>C (p.Val75=) rs367817352
NM_000218.2(KCNQ1):c.345G>A (p.Glu115=) rs758960211
NM_000218.2(KCNQ1):c.351C>T (p.Pro117=) rs764872490
NM_181798.1(KCNQ1):c.-16616T>C rs532941548
NM_181798.1(KCNQ1):c.132C>T (p.Tyr44=) rs139042529
NM_181798.1(KCNQ1):c.1335G>A (p.Leu445=) rs886039093
NM_181798.1(KCNQ1):c.1368C>T (p.Arg456=) rs200670744
NM_181798.1(KCNQ1):c.1418C>T (p.Thr473Met) rs34516117
NM_181798.1(KCNQ1):c.1419G>A (p.Thr473=) rs147091980
NM_181798.1(KCNQ1):c.1446C>T (p.Ile482=) rs377553748
NM_181798.1(KCNQ1):c.1479C>T (p.His493=) rs139893266
NM_181798.1(KCNQ1):c.1494C>T (p.Pro498=) rs112113213
NM_181798.1(KCNQ1):c.1521C>T (p.Gly507=) rs774046442
NM_181798.1(KCNQ1):c.1545C>T (p.Cys515=) rs12720454
NM_181798.1(KCNQ1):c.261C>T (p.Cys87=) rs775479779
NM_181798.1(KCNQ1):c.423C>T (p.Ile141=) rs373227792
NM_181798.1(KCNQ1):c.430C>T (p.Leu144=) rs189991547
NM_181798.1(KCNQ1):c.603C>T (p.Ile201=) rs140019543
NM_181798.1(KCNQ1):c.66C>T (p.Ala22=) rs146436765
NM_181798.1(KCNQ1):c.78G>A (p.Thr26=) rs148121889
NM_181798.1(KCNQ1):c.951G>A (p.Thr317=) rs144985256
NM_181798.1(KCNQ1):c.975G>T (p.Arg325=) rs753619991

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