EGFR c.2701+2093T>C

Variant ID: 7-55262627-T-C

NM_005228.3(EGFR):c.2701+2093T>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: rs1404908
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



A two-stage case-control study of EGFR polymorphisms and breast cancer risk.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Hong, Young-Seoub YS; Deming, Sandra L SL; Gao, Yu-Tang YT; Long, Ji-Rong JR; Shu, Xiao-Ou XO; Cai, Qiuyin Q; Lu, Wei W; Zheng, Wei W
Publication Date: 2009-02

Variant appearance in text: rs1404908
PubMed Link: 19190167
Variant Present in the following documents:
  • Main text
View BVdb publication page