rs3917639
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs3917639(A;A) |
| Make rs3917639(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 94527220 |
| Gene | F3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3917639 |
| dbSNP (classic) | rs3917639 |
| ClinGen | rs3917639 |
| ebi | rs3917639 |
| HLI | rs3917639 |
| Exac | rs3917639 |
| Gnomad | rs3917639 |
| Varsome | rs3917639 |
| LitVar | rs3917639 |
| Map | rs3917639 |
| PheGenI | rs3917639 |
| Biobank | rs3917639 |
| 1000 genomes | rs3917639 |
| hgdp | rs3917639 |
| ensembl | rs3917639 |
| geneview | rs3917639 |
| scholar | rs3917639 |
| rs3917639 | |
| pharmgkb | rs3917639 |
| gwascentral | rs3917639 |
| openSNP | rs3917639 |
| 23andMe | rs3917639 |
| SNPshot | rs3917639 |
| SNPdbe | rs3917639 |
| MSV3d | rs3917639 |
| GWAS Ctlg | rs3917639 |
| Max Magnitude | 0 |
[PMID 19583819] Tissue factor gene polymorphisms and haplotypes and the risk of ischemic vascular events: four studies and a meta-analysis
