rs1367228
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1367228(A;A) |
| Make rs1367228(A;C) |
| Make rs1367228(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 55885305 |
| Gene | EFEMP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1367228 |
| dbSNP (classic) | rs1367228 |
| ClinGen | rs1367228 |
| ebi | rs1367228 |
| HLI | rs1367228 |
| Exac | rs1367228 |
| Gnomad | rs1367228 |
| Varsome | rs1367228 |
| LitVar | rs1367228 |
| Map | rs1367228 |
| PheGenI | rs1367228 |
| Biobank | rs1367228 |
| 1000 genomes | rs1367228 |
| hgdp | rs1367228 |
| ensembl | rs1367228 |
| geneview | rs1367228 |
| scholar | rs1367228 |
| rs1367228 | |
| pharmgkb | rs1367228 |
| gwascentral | rs1367228 |
| openSNP | rs1367228 |
| 23andMe | rs1367228 |
| SNPshot | rs1367228 |
| SNPdbe | rs1367228 |
| MSV3d | rs1367228 |
| GWAS Ctlg | rs1367228 |
| GMAF | 0.3627 |
| 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 | T |
| P-val | 2E-9 |
| Odds Ratio | 1.49 [NR] |
