CYP2C9 c.168+318G>T

Variant ID: 10-96698925-G-T

NM_000771.3(CYP2C9):c.168+318G>T

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: rs9332105
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Cytochrome P450 2C9 (CYP2C9) polymorphisms in Chinese Li population.

International Journal Of Clinical And Experimental Medicine
Ding, Yipeng Y; Yang, Danlei D; Zhou, Long L; He, Ping P; Yao, Jinjian J; Xie, Pingdong P; Lin, Daobo D; Sun, Dingwei D; Sun, Pei P; Li, Quanni Q; Geng, Tingting T; Jin, Tianbo T
Publication Date: 2015

Variant appearance in text: rs9332105
PubMed Link: 26885033
Variant Present in the following documents:
  • Main text
View BVdb publication page