SCN5A c.611+3059C>A

Variant ID: 3-38659275-G-T

NM_000335.4(SCN5A):c.611+3059C>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs7637849
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Replication of SCN5A Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies.

Evolutionary Computation, Machine Learning And Data Mining In Bioinformatics. Evobio (Conference)
Jeff, Janina M JM; Brown-Gentry, Kristin K; Goodloe, Robert R; Ritchie, Marylyn D MD; Denny, Joshua C JC; Kho, Abel N AN; Armstrong, Loren L LL; McClellan, Bob B; Mayo, Ping P; Allen, Melissa M; Jin, Hailing H; Gillani, Niloufar B NB; Schnetz-Boutaud, Nathalie N; Dilks, Holli H HH; Basford, Melissa A MA; Pacheco, Jennifer A JA; Jarvik, Gail P GP; Chisholm, Rex L RL; Roden, Dan M DM; Hayes, M Geoffrey MG; Crawford, Dana C DC
Publication Date: 2014

Variant appearance in text: rs7637849
PubMed Link: 25590050
Variant Present in the following documents:
  • Main text
View BVdb publication page