Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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