ClinVar Miner

List of variants in gene KCNQ1 studied for Arrhythmia

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Total variants: 59
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HGVS dbSNP
NM_181798.1(KCNQ1):c.1007G>C (p.Ser336Thr) rs184636161
NM_181798.1(KCNQ1):c.1134-3C>T rs1564886312
NM_181798.1(KCNQ1):c.1174C>T (p.Arg392Cys) rs199472787
NM_181798.1(KCNQ1):c.1215G>A (p.Ala405=) rs558452873
NM_181798.1(KCNQ1):c.1227C>T (p.Tyr409=) rs138551008
NM_181798.1(KCNQ1):c.1240G>A (p.Val414Ile) rs199472796
NM_181798.1(KCNQ1):c.1257G>A (p.Ser419=) rs1057128
NM_181798.1(KCNQ1):c.132C>T (p.Tyr44=) rs139042529
NM_181798.1(KCNQ1):c.1339A>G (p.Ile447Val) rs761947465
NM_181798.1(KCNQ1):c.1368C>T (p.Arg456=) rs200670744
NM_181798.1(KCNQ1):c.1386C>T (p.Gly462=) rs368364062
NM_181798.1(KCNQ1):c.1419G>A (p.Thr473=) rs147091980
NM_181798.1(KCNQ1):c.1479C>T (p.His493=) rs139893266
NM_181798.1(KCNQ1):c.1545C>T (p.Cys515=) rs12720454
NM_181798.1(KCNQ1):c.1546G>A (p.Gly516Ser) rs1800172
NM_181798.1(KCNQ1):c.1561G>A (p.Val521Ile) rs34150427
NM_181798.1(KCNQ1):c.1605C>T (p.Tyr535=) rs11601907
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.222C>T (p.Ile74=) rs146190510
NM_181798.1(KCNQ1):c.291G>A (p.Thr97=) rs550887954
NM_181798.1(KCNQ1):c.339C>T (p.His113=) rs28730754
NM_181798.1(KCNQ1):c.342C>T (p.Val114=) rs1358413257
NM_181798.1(KCNQ1):c.395G>A (p.Arg132His) rs199472720
NM_181798.1(KCNQ1):c.415C>A (p.Leu139Met) rs1263583359
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.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.54C>T (p.Ile18=) rs1800170
NM_181798.1(KCNQ1):c.558C>T (p.Ile186=) rs199472747
NM_181798.1(KCNQ1):c.591C>T (p.Val197=) rs554518844
NM_181798.1(KCNQ1):c.603C>T (p.Ile201=) rs140019543
NM_181798.1(KCNQ1):c.652-12A>G rs200423553
NM_181798.1(KCNQ1):c.652-4C>T rs543599445
NM_181798.1(KCNQ1):c.66C>T (p.Ala22=) rs146436765
NM_181798.1(KCNQ1):c.728C>T (p.Ala243Val) rs775362401
NM_181798.1(KCNQ1):c.747+6G>A rs558595162
NM_181798.1(KCNQ1):c.77C>T (p.Thr26Met) rs143709408
NM_181798.1(KCNQ1):c.78G>A (p.Thr26=) rs148121889
NM_181798.1(KCNQ1):c.798G>T (p.Lys266Asn) rs12720457
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.841C>G (p.Pro281Ala) rs28730756
NM_181798.1(KCNQ1):c.871-3del rs12720450
NM_181798.1(KCNQ1):c.875A>G (p.Lys292Arg) rs757328965
NM_181798.1(KCNQ1):c.900A>G (p.Lys300=) rs763197403
NM_181798.1(KCNQ1):c.962C>G (p.Pro321Arg) rs12720449
NM_181798.1(KCNQ1):c.968A>G (p.Glu323Gly) rs1057518902
NM_181798.1(KCNQ1):c.97-10G>A rs28730752
NM_181798.1(KCNQ1):c.97-8C>T rs150711844
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.993C>T (p.Val331=) rs778598703
NM_181798.1(KCNQ1):c.994G>A (p.Asp332Asn) rs747704276
NM_181798.1(KCNQ1):c.996C>T (p.Asp332=) rs200418488
NM_181798.1(KCNQ1):c.997G>A (p.Gly333Ser) rs199472783

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