F5 c.6346-995A>T

Variant ID: 1-169485859-T-A

NM_000130.4(F5):c.6346-995A>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: rs2420369
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Combined effects of thrombosis pathway gene variants predict cardiovascular events.

Plos Genetics
Auro, Kirsi K; Alanne, Mervi M; Kristiansson, Kati K; Silander, Kaisa K; Kuulasmaa, Kari K; Salomaa, Veikko V; Peltonen, Leena L; Perola, Markus M
Publication Date: 2007-07

Variant appearance in text: rs2420369
PubMed Link: 17677000
Variant Present in the following documents:
  • Main text
  • pgen.0030120.pdf
View BVdb publication page