ClinVar Miner

List of variants in gene KCNQ1 reported as benign by GeneDx

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Gene type:
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Total variants: 45
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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.386+14C>T rs370023636
NM_000218.2(KCNQ1):c.386+15671G>A
NM_000218.2(KCNQ1):c.386+15841G>A
NM_181798.1(KCNQ1):c.-10G>A rs201090517
NM_181798.1(KCNQ1):c.-16616T>C rs532941548
NM_181798.1(KCNQ1):c.1134-218A>G
NM_181798.1(KCNQ1):c.1134-31C>G
NM_181798.1(KCNQ1):c.1209+14T>C rs11024034
NM_181798.1(KCNQ1):c.1257G>A (p.Ser419=) rs1057128
NM_181798.1(KCNQ1):c.1304+282C>T
NM_181798.1(KCNQ1):c.1305-49C>T
NM_181798.1(KCNQ1):c.1351+186A>G
NM_181798.1(KCNQ1):c.1368C>T (p.Arg456=) rs200670744
NM_181798.1(KCNQ1):c.1413+11G>A rs186188610
NM_181798.1(KCNQ1):c.1413+245T>C
NM_181798.1(KCNQ1):c.1414-119T>C
NM_181798.1(KCNQ1):c.1414-298A>G
NM_181798.1(KCNQ1):c.1479C>T (p.His493=) rs139893266
NM_181798.1(KCNQ1):c.1563C>T (p.Val521=) rs201698592
NM_181798.1(KCNQ1):c.1605C>T (p.Tyr535=) rs11601907
NM_181798.1(KCNQ1):c.171C>T (p.Tyr57=) rs780231722
NM_181798.1(KCNQ1):c.223+220A>C
NM_181798.1(KCNQ1):c.224-182T>G
NM_181798.1(KCNQ1):c.224-24C>T
NM_181798.1(KCNQ1):c.302+20T>C rs184516288
NM_181798.1(KCNQ1):c.303-234C>T
NM_181798.1(KCNQ1):c.400-19TG[2] rs727503103
NM_181798.1(KCNQ1):c.430C>T (p.Leu144=) rs189991547
NM_181798.1(KCNQ1):c.540+7C>T rs370506451
NM_181798.1(KCNQ1):c.541-228A>G
NM_181798.1(KCNQ1):c.6-18C>T rs377350869
NM_181798.1(KCNQ1):c.66C>T (p.Ala22=) rs146436765
NM_181798.1(KCNQ1):c.729G>A (p.Ala243=) rs1805118
NM_181798.1(KCNQ1):c.747+4C>T rs201590918
NM_181798.1(KCNQ1):c.748-8G>A rs200612600
NM_181798.1(KCNQ1):c.78G>A (p.Thr26=) rs148121889
NM_181798.1(KCNQ1):c.870+248G>A
NM_181798.1(KCNQ1):c.871-301T>C
NM_181798.1(KCNQ1):c.871-60G>A
NM_181798.1(KCNQ1):c.951G>A (p.Thr317=) rs144985256
NM_181798.1(KCNQ1):c.97-212C>T
NM_181798.1(KCNQ1):c.97-289_97-254dup
NM_181798.1(KCNQ1):c.97-8C>T rs150711844

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