SCN5A c.4296+116G>T

Variant ID: 3-38598606-C-A

NM_000335.4(SCN5A):c.4296+116G>T

This variant was identified in 8 publications

View GRCh38 version.




Publications:


Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06

Variant appearance in text: rs41312391
PubMed Link: 33503336
Variant Present in the following documents:
  • CNR2-4-e1335-s003.xlsx, sheet 1
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: rs41312391
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: rs41312391
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: rs41312391
PubMed Link: 30235722
Variant Present in the following documents:
  • Main text
  • medi-97-e12428.pdf
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs41312391
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



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: rs41312391
PubMed Link: 28085969
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

Plos One
Lahtinen, Annukka M AM; Noseworthy, Peter A PA; Havulinna, Aki S AS; Jula, Antti A; Karhunen, Pekka J PJ; Kettunen, Johannes J; Perola, Markus M; Kontula, Kimmo K; Newton-Cheh, Christopher C; Salomaa, Veikko V
Publication Date: 2012

Variant appearance in text: rs41312391
PubMed Link: 22844511
Variant Present in the following documents:
  • Main text
  • pone.0041675.pdf
  • pone.0041675.s005.pdf
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Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study.

Annals Of Noninvasive Electrocardiology : The Official Journal Of The International Society For Holter And Noninvasive Electrocardiology, Inc
Lehtinen, Allison B AB; Daniel, Kurt R KR; Shah, Sidharth A SA; Nelson, Matthew R MR; Ziegler, Julie T JT; Freedman, Barry I BI; Carr, J Jeffrey JJ; Herrington, David M DM; Langefeld, Carl D CD; Bowden, Donald W DW
Publication Date: 2009-01

Variant appearance in text: rs41312391
PubMed Link: 19149796
Variant Present in the following documents:
  • Main text
View BVdb publication page