rs971572
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs971572(G;G) |
| Make rs971572(G;T) |
| Make rs971572(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 184099374 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs971572 |
| dbSNP (classic) | rs971572 |
| ClinGen | rs971572 |
| ebi | rs971572 |
| HLI | rs971572 |
| Exac | rs971572 |
| Gnomad | rs971572 |
| Varsome | rs971572 |
| LitVar | rs971572 |
| Map | rs971572 |
| PheGenI | rs971572 |
| Biobank | rs971572 |
| 1000 genomes | rs971572 |
| hgdp | rs971572 |
| ensembl | rs971572 |
| geneview | rs971572 |
| scholar | rs971572 |
| rs971572 | |
| pharmgkb | rs971572 |
| gwascentral | rs971572 |
| openSNP | rs971572 |
| 23andMe | rs971572 |
| SNPshot | rs971572 |
| SNPdbe | rs971572 |
| MSV3d | rs971572 |
| GWAS Ctlg | rs971572 |
| GMAF | 0.3549 |
| Max Magnitude | 0 |
| ? | (G;G) (G;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 | |
| P-val | 9E-9 |
| Odds Ratio | 2.38 [NR] |
