Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
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: 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