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CYP2C9 c.643-115A>G
Variant ID: 10-96708750-A-G
NM_000771.3(
CYP2C9
):c.643-115A>G
This variant was identified in 3 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: rs9332129
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: rs9332129
PubMed Link:
21639946
Variant Present in the following documents:
Main text
1471-2350-12-80.pdf
View BVdb publication page
Novel variants of major drug-metabolising enzyme genes in diverse African populations and their predicted functional effects.
Human Genomics
Matimba, Alice A; Del-Favero, Jurgen J; Van Broeckhoven, Christine C; Masimirembwa, Collen C
Publication Date: 2009-01
Variant appearance in text: rs9332129
PubMed Link:
19164093
Variant Present in the following documents:
Main text
1479-7364-3-2-169.pdf
View BVdb publication page