SCN5A c.392+242T>C

Variant ID: 3-38671560-A-G

NM_000335.4(SCN5A):c.392+242T>C

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: rs45567533
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at ID2.

Heart (British Cardiac Society)
Seyerle, Amanda A AA; Lin, Henry J HJ; Gogarten, Stephanie M SM; Stilp, Adrienne A; Méndez Giráldez, Raul R; Soliman, Elsayed E; Baldassari, Antoine A; Graff, Mariaelisa M; Heckbert, Susan S; Kerr, Kathleen F KF; Kooperberg, Charles C; Rodriguez, Carlos C; Guo, Xiuqing X; Yao, Jie J; Sotoodehnia, Nona N; Taylor, Kent D KD; Whitsel, Eric A EA; Rotter, Jerome I JI; Laurie, Cathy C CC; Avery, Christy L CL
Publication Date: 2018-06

Variant appearance in text: rs45567533
PubMed Link: 29127183
Variant Present in the following documents:
  • Main text
View BVdb publication page