ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP
NM_004519.4(KCNQ3):c.*1159G>A rs117218884
NM_004519.4(KCNQ3):c.*1383C>T rs146987908
NM_004519.4(KCNQ3):c.*1384G>A rs528989294
NM_004519.4(KCNQ3):c.*1582C>T rs140360332
NM_004519.4(KCNQ3):c.*1676T>C rs574831064
NM_004519.4(KCNQ3):c.*1697C>G rs71526238
NM_004519.4(KCNQ3):c.*2010T>A rs139631143
NM_004519.4(KCNQ3):c.*2166A>G rs35279095
NM_004519.4(KCNQ3):c.*2271T>A rs149825293
NM_004519.4(KCNQ3):c.*2847T>C rs138023368
NM_004519.4(KCNQ3):c.*2876C>G rs572963665
NM_004519.4(KCNQ3):c.*3165G>T rs567074601
NM_004519.4(KCNQ3):c.*3261C>T rs181166117
NM_004519.4(KCNQ3):c.*3280G>C rs550558851
NM_004519.4(KCNQ3):c.*3303C>A rs571392133
NM_004519.4(KCNQ3):c.*3544A>G rs61190986
NM_004519.4(KCNQ3):c.*3701G>A rs576940686
NM_004519.4(KCNQ3):c.*3731G>T rs117524261
NM_004519.4(KCNQ3):c.*3823G>A rs17651980
NM_004519.4(KCNQ3):c.*3897C>G rs191691741
NM_004519.4(KCNQ3):c.*3957A>G rs16904601
NM_004519.4(KCNQ3):c.*4027G>A rs529880251
NM_004519.4(KCNQ3):c.*4043C>T rs117527951
NM_004519.4(KCNQ3):c.*4258T>C rs113937538
NM_004519.4(KCNQ3):c.*4316del rs61438560
NM_004519.4(KCNQ3):c.*4551T>C rs184864538
NM_004519.4(KCNQ3):c.*4736G>A rs114070302
NM_004519.4(KCNQ3):c.*4817G>A rs76758430
NM_004519.4(KCNQ3):c.*4949G>T rs561176499
NM_004519.4(KCNQ3):c.*5018C>G rs534993423
NM_004519.4(KCNQ3):c.*5255T>C rs146830560
NM_004519.4(KCNQ3):c.*5391C>T rs569024726
NM_004519.4(KCNQ3):c.*5482A>G rs192695801
NM_004519.4(KCNQ3):c.*5578A>G rs148780224
NM_004519.4(KCNQ3):c.*5704C>T rs145396746
NM_004519.4(KCNQ3):c.*5762G>A rs77343115
NM_004519.4(KCNQ3):c.*5965T>C rs537622929
NM_004519.4(KCNQ3):c.*6174A>G rs116373101
NM_004519.4(KCNQ3):c.*6199C>T rs183259250
NM_004519.4(KCNQ3):c.*6267T>C rs548690680
NM_004519.4(KCNQ3):c.*6446del rs35153843
NM_004519.4(KCNQ3):c.*7214G>A rs150753935
NM_004519.4(KCNQ3):c.*7331A>G rs557322356
NM_004519.4(KCNQ3):c.*7413G>C rs111267263
NM_004519.4(KCNQ3):c.*7464C>A rs35604597
NM_004519.4(KCNQ3):c.*7504C>G rs532052931
NM_004519.4(KCNQ3):c.*7689A>G rs142621198
NM_004519.4(KCNQ3):c.*7722T>A rs138128512
NM_004519.4(KCNQ3):c.*828T>C rs79953574
NM_004519.4(KCNQ3):c.-65C>T rs180674534
NM_004519.4(KCNQ3):c.-85C>T rs765522706
NM_004519.4(KCNQ3):c.1551C>T (p.Ala517=) rs35538317
NM_004519.4(KCNQ3):c.1564G>A (p.Val522Ile) rs143683496
NM_004519.4(KCNQ3):c.1656C>T (p.Ala552=) rs199722269
NM_004519.4(KCNQ3):c.1700+3G>A rs115092422
NM_004519.4(KCNQ3):c.1720C>T (p.Pro574Ser) rs74582884
NM_004519.4(KCNQ3):c.1737G>A (p.Thr579=) rs574981327
NM_004519.4(KCNQ3):c.1958A>G (p.Gln653Arg) rs554833870
NM_004519.4(KCNQ3):c.2071G>A (p.Gly691Ser) rs747379988
NM_004519.4(KCNQ3):c.2262C>T (p.Leu754=) rs555827251
NM_004519.4(KCNQ3):c.2263G>A (p.Asp755Asn) rs150821246
NM_004519.4(KCNQ3):c.2306C>A (p.Pro769His) rs114095081
NM_004519.4(KCNQ3):c.2330G>A (p.Arg777Gln) rs201328910
NM_004519.4(KCNQ3):c.2349G>A (p.Thr783=) rs145063831
NM_004519.4(KCNQ3):c.2462A>G (p.Asn821Ser) rs118192254
NM_004519.4(KCNQ3):c.948C>T (p.Thr316=) rs142144538

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