EGFR c.89-34103A>G

Variant ID: 7-55175876-A-G

NM_005228.3(EGFR):c.89-34103A>G

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: rs7796139
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



An analysis of growth, differentiation and apoptosis genes with risk of renal cancer.

Plos One
Dong, Linda M LM; Brennan, Paul P; Karami, Sara S; Hung, Rayjean J RJ; Menashe, Idan I; Berndt, Sonja I SI; Yeager, Meredith M; Chanock, Stephen S; Zaridze, David D; Matveev, Vsevolod V; Janout, Vladimir V; Kollarova, Hellena H; Bencko, Vladimir V; Schwartz, Kendra K; Davis, Faith F; Navratilova, Marie M; Szeszenia-Dabrowska, Neonila N; Mates, Dana D; Colt, Joanne S JS; Holcatova, Ivana I; Boffetta, Paolo P; Rothman, Nathaniel N; Chow, Wong-Ho WH; Rosenberg, Philip S PS; Moore, Lee E LE
Publication Date: 2009-03-24

Variant appearance in text: rs7796139
PubMed Link: 19603096
Variant Present in the following documents:
  • Main text
  • pone.0004895.pdf
View BVdb publication page