rs2036914
| Orientation | plus |
| Stabilized | plus |
| Make rs2036914(C;C) |
| Make rs2036914(C;T) |
| Make rs2036914(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 186271327 |
| Gene | F11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2036914 |
| dbSNP (classic) | rs2036914 |
| ClinGen | rs2036914 |
| ebi | rs2036914 |
| HLI | rs2036914 |
| Exac | rs2036914 |
| Gnomad | rs2036914 |
| Varsome | rs2036914 |
| LitVar | rs2036914 |
| Map | rs2036914 |
| PheGenI | rs2036914 |
| Biobank | rs2036914 |
| 1000 genomes | rs2036914 |
| hgdp | rs2036914 |
| ensembl | rs2036914 |
| geneview | rs2036914 |
| scholar | rs2036914 |
| rs2036914 | |
| pharmgkb | rs2036914 |
| gwascentral | rs2036914 |
| openSNP | rs2036914 |
| 23andMe | rs2036914 |
| SNPshot | rs2036914 |
| SNPdbe | rs2036914 |
| MSV3d | rs2036914 |
| GWAS Ctlg | rs2036914 |
| GMAF | 0.3678 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19583818] Genetic variants associated with deep vein thrombosis: the F11 locus
[PMID 21232005
] New gene variants associated with venous thrombosis: a replication study in White and Black Americans.
[PMID 23150947] Single nucleotide polymorphisms and the risk of venous thrombosis: results from a Danish case-cohort study
[PMID 25210051] Genetic Variations Associated with Recurrent Venous Thrombosis
[PMID 29094466] Joint effects of prothrombotic genotypes and body height on the risk of venous thromboembolism: The Tromsø Study.
[PMID 30773804] Effect of prothrombotic genotypes on the risk of venous thromboembolism in patients with and without ischemic stroke.The TromsØ Study.
[PMID 32110755] Myocardial infarction, prothrombotic genotypes, and venous thrombosis risk: The Tromsø Study.
[PMID 32402998] Prothrombotic genotypes and risk of major bleeding in patients with incident venous thromboembolism.
[PMID 32671915] Combined effects of five prothrombotic genotypes and cancer on the risk of a first venous thromboembolic event.
