rs2028385
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2028385(A;A) |
| Make rs2028385(A;G) |
| Make rs2028385(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 96423644 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2028385 |
| dbSNP (classic) | rs2028385 |
| ClinGen | rs2028385 |
| ebi | rs2028385 |
| HLI | rs2028385 |
| Exac | rs2028385 |
| Gnomad | rs2028385 |
| Varsome | rs2028385 |
| LitVar | rs2028385 |
| Map | rs2028385 |
| PheGenI | rs2028385 |
| Biobank | rs2028385 |
| 1000 genomes | rs2028385 |
| hgdp | rs2028385 |
| ensembl | rs2028385 |
| geneview | rs2028385 |
| scholar | rs2028385 |
| rs2028385 | |
| pharmgkb | rs2028385 |
| gwascentral | rs2028385 |
| openSNP | rs2028385 |
| 23andMe | rs2028385 |
| SNPshot | rs2028385 |
| SNPdbe | rs2028385 |
| MSV3d | rs2028385 |
| GWAS Ctlg | rs2028385 |
| GMAF | 0.2296 |
| 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 | C |
| P-val | 9E-9 |
| Odds Ratio | 1.69 [NR] |
