EGFR c.88+41673A>G

Variant ID: 7-55128731-A-G

NM_005228.3(EGFR):c.88+41673A>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: rs1024750
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
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: rs1024750
PubMed Link: 25396734
Variant Present in the following documents:
  • Main text
  • pone.0112358.pdf
View BVdb publication page