EGF c.3173+1494T>C

Variant ID: 4-110922496-T-C

NM_001963.4(EGF):c.3173+1494T>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: rs2282786
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide Approach.

Biomed Research International
Kim, Yun Kyoung YK; Oh, Ji Hee JH; Kim, Young Jin YJ; Hwang, Mi Yeong MY; Moon, Sanghoon S; Low, Siew-Kee SK; Takahashi, Atsushi A; Matsuda, Koichi K; Kubo, Michiaki M; Lee, Juyoung J; Kim, Bong-Jo BJ
Publication Date: 2015

Variant appearance in text: rs2282786
PubMed Link: 26064965
Variant Present in the following documents:
  • Main text
  • BMRI2015-914965.pdf
View BVdb publication page