ClinVar Miner

List of variants in gene KCNQ3 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_004519.4(KCNQ3):c.*2166A>G rs35279095 0.02440
NM_004519.4(KCNQ3):c.*6446del rs35153843 0.02379
NM_004519.4(KCNQ3):c.*1697C>G rs71526238 0.02377
NM_004519.4(KCNQ3):c.*7464C>A rs35604597 0.02371
NM_004519.4(KCNQ3):c.*4316del rs61438560 0.01792
NM_004519.4(KCNQ3):c.*7413G>C rs111267263 0.01573
NM_004519.4(KCNQ3):c.1700+3G>A rs115092422 0.01419
NM_004519.4(KCNQ3):c.*1383C>T rs146987908 0.01123
NM_004519.4(KCNQ3):c.*4258T>C rs113937538 0.01032
NM_004519.4(KCNQ3):c.*3823G>A rs17651980 0.00951
NM_004519.4(KCNQ3):c.*3957A>G rs16904601 0.00945
NM_004519.4(KCNQ3):c.*5255T>C rs146830560 0.00938
NM_004519.4(KCNQ3):c.1551C>T (p.Ala517=) rs35538317 0.00761
NM_004519.4(KCNQ3):c.*5762G>A rs77343115 0.00723
NM_004519.4(KCNQ3):c.2306C>A (p.Pro769His) rs114095081 0.00702
NM_004519.4(KCNQ3):c.*4736G>A rs114070302 0.00623
NM_004519.4(KCNQ3):c.*4817G>A rs76758430 0.00586
NM_004519.4(KCNQ3):c.948C>T (p.Thr316=) rs142144538 0.00564
NM_004519.4(KCNQ3):c.-65C>T rs180674534 0.00507
NM_004519.4(KCNQ3):c.*5704C>T rs145396746 0.00474
NM_004519.4(KCNQ3):c.*6174A>G rs116373101 0.00433
NM_004519.4(KCNQ3):c.*3731G>T rs117524261 0.00428
NM_004519.4(KCNQ3):c.*3544A>G rs61190986 0.00393
NM_004519.4(KCNQ3):c.*3701G>A rs576940686 0.00391
NM_004519.4(KCNQ3):c.*5578A>G rs148780224 0.00381
NM_004519.4(KCNQ3):c.*7689A>G rs142621198 0.00377
NM_004519.4(KCNQ3):c.*6199C>T rs183259250 0.00240
NM_004519.4(KCNQ3):c.*7722T>A rs138128512 0.00213
NM_004519.4(KCNQ3):c.*4949G>T rs561176499 0.00201
NM_004519.4(KCNQ3):c.*3303C>A rs571392133 0.00185
NM_004519.4(KCNQ3):c.*4043C>T rs117527951 0.00184
NM_004519.4(KCNQ3):c.*2271T>A rs149825293 0.00182
NM_004519.4(KCNQ3):c.*3897C>G rs191691741 0.00166
NM_004519.4(KCNQ3):c.*2847T>C rs138023368 0.00156
NM_004519.4(KCNQ3):c.*5965T>C rs537622929 0.00150
NM_004519.4(KCNQ3):c.*1384G>A rs528989294 0.00131
NM_004519.4(KCNQ3):c.*3165G>T rs567074601 0.00091
NM_004519.4(KCNQ3):c.*828T>C rs79953574 0.00091
NM_004519.4(KCNQ3):c.*1159G>A rs117218884 0.00087
NM_004519.4(KCNQ3):c.*2876C>G rs572963665 0.00085
NM_004519.4(KCNQ3):c.*1582C>T rs140360332 0.00058
NM_004519.4(KCNQ3):c.*4551T>C rs184864538 0.00053
NM_004519.4(KCNQ3):c.*3280G>C rs550558851 0.00051
NM_004519.4(KCNQ3):c.-85C>T rs765522706 0.00043
NM_004519.4(KCNQ3):c.2349G>A (p.Thr783=) rs145063831 0.00043
NM_004519.4(KCNQ3):c.*2010T>A rs139631143 0.00037
NM_004519.4(KCNQ3):c.2330G>A (p.Arg777Gln) rs201328910 0.00034
NM_004519.4(KCNQ3):c.2263G>A (p.Asp755Asn) rs150821246 0.00031
NM_004519.4(KCNQ3):c.*5018C>G rs534993423 0.00029
NM_004519.4(KCNQ3):c.*5391C>T rs569024726 0.00021
NM_004519.4(KCNQ3):c.2462A>G (p.Asn821Ser) rs118192254 0.00021
NM_004519.4(KCNQ3):c.*7214G>A rs150753935 0.00010
NM_004519.4(KCNQ3):c.*7331A>G rs557322356 0.00009
NM_004519.4(KCNQ3):c.1568+14G>A rs370848714 0.00007
NM_004519.4(KCNQ3):c.1656C>T (p.Ala552=) rs199722269 0.00006
NM_004519.4(KCNQ3):c.*7504C>G rs532052931 0.00005
NM_004519.4(KCNQ3):c.*5482A>G rs192695801 0.00004
NM_004519.4(KCNQ3):c.1564G>A (p.Val522Ile) rs143683496 0.00004
NM_004519.4(KCNQ3):c.616C>T (p.Leu206=) rs770952684 0.00004
NM_004519.4(KCNQ3):c.*1676T>C rs574831064 0.00003
NM_004519.4(KCNQ3):c.*4027G>A rs529880251 0.00002
NM_004519.4(KCNQ3):c.1507G>A (p.Gly503Arg) rs773584143 0.00002
NM_004519.4(KCNQ3):c.1623C>T (p.Tyr541=) rs138900075 0.00002
NM_004519.4(KCNQ3):c.1737G>A (p.Thr579=) rs574981327 0.00002
NM_004519.4(KCNQ3):c.2071G>A (p.Gly691Ser) rs747379988 0.00002
NM_004519.4(KCNQ3):c.*6267T>C rs548690680 0.00001
NM_004519.4(KCNQ3):c.2492G>A (p.Arg831Gln) rs149004528 0.00001
NM_004519.4(KCNQ3):c.*3261C>T rs181166117
NM_004519.4(KCNQ3):c.1656C>A (p.Ala552=) rs199722269
NM_004519.4(KCNQ3):c.1720C>T (p.Pro574Ser) rs74582884
NM_004519.4(KCNQ3):c.1958A>G (p.Gln653Arg) rs554833870
NM_004519.4(KCNQ3):c.2262C>T (p.Leu754=) rs555827251

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