CYP2C9 c.1149+370G>C

Variant ID: 10-96741497-G-C

NM_000771.3(CYP2C9):c.1149+370G>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: rs9332198
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Inactive alleles of cytochrome P450 2C19 may be positively selected in human evolution.

Bmc Evolutionary Biology
Janha, Ramatoulie E RE; Worwui, Archibald A; Linton, Kenneth J KJ; Shaheen, Seif O SO; Sisay-Joof, Fatoumatta F; Walton, Robert T RT
Publication Date: 2014-04-01

Variant appearance in text: rs9332198
PubMed Link: 24690327
Variant Present in the following documents:
  • Main text
  • 1471-2148-14-71.pdf
View BVdb publication page