KRAS c.450+2219T>C

Variant ID: 12-25376329-A-G

NM_004985.3(KRAS):c.450+2219T>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: rs11047901
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.

Human Reproduction Update
Tempfer, C B CB; Simoni, M M; Destenaves, B B; Fauser, B C J M BC
Publication Date: 2009

Variant appearance in text: rs11047901
PubMed Link: 18805939
Variant Present in the following documents:
  • Main text
  • dmn040.pdf
View BVdb publication page