KCNQ1 c.1515-34473T>C

Variant ID: 11-2755601-T-C

NM_000218.2(KCNQ1):c.1515-34473T>C

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Role of non-coding variants in cardiovascular disease.

Journal Of Cellular And Molecular Medicine
Heshmatzad, Katayoun K; Naderi, Niloofar N; Maleki, Majid M; Abbasi, Shiva S; Ghasemi, Serwa S; Ashrafi, Nooshin N; Fazelifar, Amir Farjam AF; Mahdavi, Mohammad M; Kalayinia, Samira S
Publication Date: 2023-05-15

Variant appearance in text: rs2283222
PubMed Link: 37183561
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sudden Cardiac Death (SCD) - risk stratification and prediction with molecular biomarkers.

Journal Of Biomedical Science
Osman, Junaida J; Tan, Shing Cheng SC; Lee, Pey Yee PY; Low, Teck Yew TY; Jamal, Rahman R
Publication Date: 2019-05-22

Variant appearance in text: rs2283222
PubMed Link: 31118017
Variant Present in the following documents:
  • Main text
  • 12929_2019_Article_535.pdf
View BVdb publication page



Usefulness of Single Nucleotide Polymorphisms as Predictors of Sudden Cardiac Death.

The American Journal Of Cardiology
Tamariz, Leonardo L; Balda, Javier J; Pareja, Dennise D; Palacio, Ana A; Myerburg, Robert J RJ; Conway, Douglas D; Davis, Lea L; Goldberger, Jeffrey J JJ
Publication Date: 2019-06-15

Variant appearance in text: rs2283222
PubMed Link: 31053292
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations between common ion channel single nucleotide polymorphisms and sudden cardiac death in adults: A MOOSE-compliant meta-analysis.

Medicine
Liu, Xiaoli X; Shi, Jianli J; Xiao, Peilin P
Publication Date: 2018-09

Variant appearance in text: rs2283222
PubMed Link: 30235722
Variant Present in the following documents:
  • Main text
  • medi-97-e12428.pdf
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A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.

Plos One
Jabbari, Reza R; Glinge, Charlotte C; Jabbari, Javad J; Risgaard, Bjarke B; Winkel, Bo Gregers BG; Terkelsen, Christian Juhl CJ; Tilsted, Hans-Henrik HH; Jensen, Lisette Okkels LO; Hougaard, Mikkel M; Haunsø, Stig S; Engstrøm, Thomas T; Albert, Christine M CM; Tfelt-Hansen, Jacob J
Publication Date: 2017

Variant appearance in text: rs2283222
PubMed Link: 28085969
Variant Present in the following documents:
  • Main text
View BVdb publication page



Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction.

Journal Of Geriatric Cardiology : Jgc
Glinge, Charlotte C; Sattler, Stefan S; Jabbari, Reza R; Tfelt-Hansen, Jacob J
Publication Date: 2016-09

Variant appearance in text: rs2283222
PubMed Link: 27899944
Variant Present in the following documents:
  • Main text
  • jgc-13-09-789.pdf
View BVdb publication page



Genetic mutation in Korean patients of sudden cardiac arrest as a surrogating marker of idiopathic ventricular arrhythmia.

Journal Of Korean Medical Science
Son, Myoung Kyun MK; Ki, Chang-Seok CS; Park, Seung-Jung SJ; Huh, June J; Kim, June Soo JS; On, Young Keun YK
Publication Date: 2013-07

Variant appearance in text: rs2283222
PubMed Link: 23853484
Variant Present in the following documents:
  • Main text
  • jkms-28-1021.pdf
View BVdb publication page



Common variants in cardiac ion channel genes are associated with sudden cardiac death.

Circulation. Arrhythmia And Electrophysiology
Albert, Christine M CM; MacRae, Calum A CA; Chasman, Daniel I DI; VanDenburgh, Martin M; Buring, Julie E JE; Manson, JoAnn E JE; Cook, Nancy R NR; Newton-Cheh, Christopher C
Publication Date: 2010-06

Variant appearance in text: rs2283222
PubMed Link: 20400777
Variant Present in the following documents:
  • Main text
View BVdb publication page