EGFR c.89-20764G>T

Variant ID: 7-55189215-G-T

NM_005228.3(EGFR):c.89-20764G>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci.

Human Genetics
Shah, Rupal L RL; Guggenheim, Jeremy A JA; ,
Publication Date: 2018-12

Variant appearance in text: rs17172445
PubMed Link: 30306274
Variant Present in the following documents:
  • Main text
  • 439_2018_Article_1942.pdf
View BVdb publication page



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: rs17172445
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page