rs2519093
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| Make rs2519093(C;T) |
| Make rs2519093(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 133266456 |
| Gene | ABO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2519093 |
| dbSNP (classic) | rs2519093 |
| ClinGen | rs2519093 |
| ebi | rs2519093 |
| HLI | rs2519093 |
| Exac | rs2519093 |
| Gnomad | rs2519093 |
| Varsome | rs2519093 |
| LitVar | rs2519093 |
| Map | rs2519093 |
| PheGenI | rs2519093 |
| Biobank | rs2519093 |
| 1000 genomes | rs2519093 |
| hgdp | rs2519093 |
| ensembl | rs2519093 |
| geneview | rs2519093 |
| scholar | rs2519093 |
| rs2519093 | |
| pharmgkb | rs2519093 |
| gwascentral | rs2519093 |
| openSNP | rs2519093 |
| 23andMe | rs2519093 |
| SNPshot | rs2519093 |
| SNPdbe | rs2519093 |
| MSV3d | rs2519093 |
| GWAS Ctlg | rs2519093 |
| Max Magnitude | 0 |
Note: this SNP does not map to reference assembly GRCh38.
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22672568 ]
|
| Trait | |
| Title | A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. |
| Risk Allele | A |
| P-val | 8E-16 |
| Odds Ratio | 1.6900 None |
[PMID 21463476] Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism.
