rs3917629
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3917629(-;-) |
Make rs3917629(-;G) |
Make rs3917629(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 94532195 |
Gene | F3 |
is a | snp |
is | mentioned by |
dbSNP | rs3917629 |
dbSNP (classic) | rs3917629 |
ClinGen | rs3917629 |
ebi | rs3917629 |
HLI | rs3917629 |
Exac | rs3917629 |
Gnomad | rs3917629 |
Varsome | rs3917629 |
LitVar | rs3917629 |
Map | rs3917629 |
PheGenI | rs3917629 |
Biobank | rs3917629 |
1000 genomes | rs3917629 |
hgdp | rs3917629 |
ensembl | rs3917629 |
geneview | rs3917629 |
scholar | rs3917629 |
rs3917629 | |
pharmgkb | rs3917629 |
gwascentral | rs3917629 |
openSNP | rs3917629 |
23andMe | rs3917629 |
SNPshot | rs3917629 |
SNPdbe | rs3917629 |
MSV3d | rs3917629 |
GWAS Ctlg | rs3917629 |
Max Magnitude | 0 |
[PMID 19583819] Tissue factor gene polymorphisms and haplotypes and the risk of ischemic vascular events: four studies and a meta-analysis