CYP2C9 c.819+3102T>C

Variant ID: 10-96712143-T-C

NM_000771.3(CYP2C9):c.819+3102T>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: rs35511771
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Pharmacogenomics of warfarin in populations of African descent.

British Journal Of Clinical Pharmacology
Suarez-Kurtz, Guilherme G; Botton, Mariana R MR
Publication Date: 2013-02

Variant appearance in text: rs35511771
PubMed Link: 22676711
Variant Present in the following documents:
  • Main text
View BVdb publication page