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PTGS1 c.762+397G>T
Variant ID: 9-125144423-G-T
NM_000962.3(
PTGS1
):c.762+397G>T
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: rs10306150
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Associations between gene polymorphisms in fatty acid metabolism pathway and preterm delivery in a US urban black population.
Human Genetics
Liu, Xin X; Wang, Guoying G; Hong, Xiumei X; Tsai, Hui-Ju HJ; Liu, Rong R; Zhang, Shanchun S; Wang, Hongjian H; Pearson, Colleen C; Ortiz, Katherin K; Wang, Deli D; Hirsch, Emmet E; Zuckerman, Barry B; Wang, Xiaobin X
Publication Date: 2012-03
Variant appearance in text: rs10306150
PubMed Link:
21847588
Variant Present in the following documents:
Main text
View BVdb publication page