Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
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: 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