SCN5A c.3837+432T>C

Variant ID: 3-38607468-A-G

NM_000335.4(SCN5A):c.3837+432T>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Concealed Substrates in Brugada Syndrome: Isolated Channelopathy or Associated Cardiomyopathy?

Genes
Di Resta, Chiara C; Berg, Jan J; Villatore, Andrea A; Maia, Marianna M; Pili, Gianluca G; Fioravanti, Francesco F; Tomaiuolo, Rossella R; Sala, Simone S; Benedetti, Sara S; Peretto, Giovanni G
Publication Date: 2022-09-28

Variant appearance in text: rs62241190
PubMed Link: 36292641
Variant Present in the following documents:
  • Main text
  • genes-13-01755.pdf
View BVdb publication page



GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations.

Plos One
Swenson, Brenton R BR; Louie, Tin T; Lin, Henry J HJ; Méndez-Giráldez, Raúl R; Below, Jennifer E JE; Laurie, Cathy C CC; Kerr, Kathleen F KF; Highland, Heather H; Thornton, Timothy A TA; Ryckman, Kelli K KK; Kooperberg, Charles C; Soliman, Elsayed Z EZ; Seyerle, Amanda A AA; Guo, Xiuqing X; Taylor, Kent D KD; Yao, Jie J; Heckbert, Susan R SR; Darbar, Dawood D; Petty, Lauren E LE; McKnight, Barbara B; Cheng, Susan S; Bello, Natalie A NA; Whitsel, Eric A EA; Hanis, Craig L CL; Nalls, Mike A MA; Evans, Daniel S DS; Rotter, Jerome I JI; Sofer, Tamar T; Avery, Christy L CL; Sotoodehnia, Nona N
Publication Date: 2019

Variant appearance in text: rs62241190
PubMed Link: 31251759
Variant Present in the following documents:
  • Main text
  • pone.0217796.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: rs62241190
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page