rs315122
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs315122(A;A) |
| Make rs315122(A;C) |
| Make rs315122(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 12 |
| Position | 69377293 |
| Gene | YEATS4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs315122 |
| dbSNP (classic) | rs315122 |
| ClinGen | rs315122 |
| ebi | rs315122 |
| HLI | rs315122 |
| Exac | rs315122 |
| Gnomad | rs315122 |
| Varsome | rs315122 |
| LitVar | rs315122 |
| Map | rs315122 |
| PheGenI | rs315122 |
| Biobank | rs315122 |
| 1000 genomes | rs315122 |
| hgdp | rs315122 |
| ensembl | rs315122 |
| geneview | rs315122 |
| scholar | rs315122 |
| rs315122 | |
| pharmgkb | rs315122 |
| gwascentral | rs315122 |
| openSNP | rs315122 |
| 23andMe | rs315122 |
| SNPshot | rs315122 |
| SNPdbe | rs315122 |
| MSV3d | rs315122 |
| GWAS Ctlg | rs315122 |
| GMAF | 0.23 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 1E-9 |
| Odds Ratio | 2.05 [NR] |
