rs9804128
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9804128(A;A) |
| Make rs9804128(A;G) |
| Make rs9804128(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 18098517 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9804128 |
| dbSNP (classic) | rs9804128 |
| ClinGen | rs9804128 |
| ebi | rs9804128 |
| HLI | rs9804128 |
| Exac | rs9804128 |
| Gnomad | rs9804128 |
| Varsome | rs9804128 |
| LitVar | rs9804128 |
| Map | rs9804128 |
| PheGenI | rs9804128 |
| Biobank | rs9804128 |
| 1000 genomes | rs9804128 |
| hgdp | rs9804128 |
| ensembl | rs9804128 |
| geneview | rs9804128 |
| scholar | rs9804128 |
| rs9804128 | |
| pharmgkb | rs9804128 |
| gwascentral | rs9804128 |
| openSNP | rs9804128 |
| 23andMe | rs9804128 |
| SNPshot | rs9804128 |
| SNPdbe | rs9804128 |
| MSV3d | rs9804128 |
| GWAS Ctlg | rs9804128 |
| GMAF | 0.3017 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | A |
| P-val | 2E-9 |
| Odds Ratio | 1.71 [NR] |
