rs1423386
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1423386(C;C) |
| Make rs1423386(C;T) |
| Make rs1423386(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 62689026 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1423386 |
| dbSNP (classic) | rs1423386 |
| ClinGen | rs1423386 |
| ebi | rs1423386 |
| HLI | rs1423386 |
| Exac | rs1423386 |
| Gnomad | rs1423386 |
| Varsome | rs1423386 |
| LitVar | rs1423386 |
| Map | rs1423386 |
| PheGenI | rs1423386 |
| Biobank | rs1423386 |
| 1000 genomes | rs1423386 |
| hgdp | rs1423386 |
| ensembl | rs1423386 |
| geneview | rs1423386 |
| scholar | rs1423386 |
| rs1423386 | |
| pharmgkb | rs1423386 |
| gwascentral | rs1423386 |
| openSNP | rs1423386 |
| 23andMe | rs1423386 |
| SNPshot | rs1423386 |
| SNPdbe | rs1423386 |
| MSV3d | rs1423386 |
| GWAS Ctlg | rs1423386 |
| GMAF | 0.2287 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23509962 ]
|
| Trait | Venous thromboembolism (gene x gene interaction) |
| Title | A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. |
| Risk Allele | G |
| P-val | 2E-9 |
| Odds Ratio | 1.73 [NR] |
