EGFR c.88+18262A>G

Variant ID: 7-55105320-A-G

NM_005228.3(EGFR):c.88+18262A>G

This variant was identified in 3 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: rs12718939
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetic Basis of Irritant Susceptibility in Health Care Workers.

Journal Of Occupational And Environmental Medicine
Yucesoy, Berran B; Talzhanov, Yerkebulan Y; Barmada, M Michael MM; Johnson, Victor J VJ; Kashon, Michael L ML; Baron, Elma E; Wilson, Nevin W NW; Frye, Bonnie B; Wang, Wei W; Fluharty, Kara K; Gharib, Rola R; Meade, Jean J; Germolec, Dori D; Luster, Michael I MI; Nedorost, Susan S
Publication Date: 2016-08

Variant appearance in text: rs12718939
PubMed Link: 27206134
Variant Present in the following documents:
  • Main text
View BVdb publication page



Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women.

Plos One
Zhou, Qiu-Hong QH; Zhao, Lan-Juan LJ; Wang, Ping P; Badr, Rhamee R; Xu, Xiao-Jing XJ; Bu, Feng-Xiao FX; Lappe, Joan J; Recker, Robert R; Zhou, Yu Y; Ye, An A; Zhou, Bo-Ting BT
Publication Date: 2014

Variant appearance in text: rs12718939
PubMed Link: 25396734
Variant Present in the following documents:
  • Main text
  • pone.0112358.pdf
View BVdb publication page