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.




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