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CYP2C8 c.1292-204A>G
Variant ID: 10-96797270-T-C
NM_000770.3(
CYP2C8
):c.1292-204A>G
This variant was identified in 4 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: rs11572177
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Screening for 392 polymorphisms in 141 pharmacogenes.
Biomedical Reports
Kim, Jason Yongha JY; Cheong, Hyun Sub HS; Park, Tae-Joon TJ; Shin, Hee Jung HJ; Seo, Doo Won DW; Na, Han Sung HS; Chung, Myeon Woo MW; Shin, Hyoung Doo HD
Publication Date: 2014-07
Variant appearance in text: rs11572177
PubMed Link:
24944790
Variant Present in the following documents:
Main text
View BVdb publication page
Genetic determinants of hair and eye colours in the Scottish and Danish populations.
Bmc Genetics
Mengel-From, Jonas J; Wong, Terence H TH; Morling, Niels N; Rees, Jonathan L JL; Jackson, Ian J IJ
Publication Date: 2009-12-30
Variant appearance in text: rs11572177
PubMed Link:
20042077
Variant Present in the following documents:
Main text
1471-2156-10-88.pdf
View BVdb publication page