CYP2C9 c.481+374A>G

Variant ID: 10-96702472-A-G

NM_000771.3(CYP2C9):c.481+374A>G

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: rs28371677
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetic factors associated with patient-specific warfarin dose in ethnic Indonesians.

Bmc Medical Genetics
Suriapranata, Ivet M IM; Tjong, Wen Ye WY; Wang, Tingliang T; Utama, Andi A; Raharjo, Sunu B SB; Yuniadi, Yoga Y; Tai, Susan Sw SS
Publication Date: 2011-06-06

Variant appearance in text: rs28371677
PubMed Link: 21639946
Variant Present in the following documents:
  • Main text
  • 1471-2350-12-80.pdf
View BVdb publication page