PTGIS c.1358+389A>G

Variant ID: 20-48127176-T-C

NM_000961.3(PTGIS):c.1358+389A>G

This variant was identified in 3 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: rs729824
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Variation in eicosanoid genes, non-fatal myocardial infarction and ischemic stroke.

Atherosclerosis
Lemaitre, Rozenn N RN; Rice, Kenneth K; Marciante, Kristin K; Bis, Joshua C JC; Lumley, Thomas S TS; Wiggins, Kerri L KL; Smith, Nicholas L NL; Heckbert, Susan R SR; Psaty, Bruce M BM
Publication Date: 2009-06

Variant appearance in text: rs729824
PubMed Link: 19046748
Variant Present in the following documents:
  • Main text
View BVdb publication page