rs10476160
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10476160(A;A) |
| Make rs10476160(A;G) |
| Make rs10476160(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 175547573 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10476160 |
| dbSNP (classic) | rs10476160 |
| ClinGen | rs10476160 |
| ebi | rs10476160 |
| HLI | rs10476160 |
| Exac | rs10476160 |
| Gnomad | rs10476160 |
| Varsome | rs10476160 |
| LitVar | rs10476160 |
| Map | rs10476160 |
| PheGenI | rs10476160 |
| Biobank | rs10476160 |
| 1000 genomes | rs10476160 |
| hgdp | rs10476160 |
| ensembl | rs10476160 |
| geneview | rs10476160 |
| scholar | rs10476160 |
| rs10476160 | |
| pharmgkb | rs10476160 |
| gwascentral | rs10476160 |
| openSNP | rs10476160 |
| 23andMe | rs10476160 |
| SNPshot | rs10476160 |
| SNPdbe | rs10476160 |
| MSV3d | rs10476160 |
| GWAS Ctlg | rs10476160 |
| GMAF | 0.3173 |
| 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 | |
| P-val | 9E-9 |
| Odds Ratio | 1.61 [NR] |
