Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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