rs687289
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs687289(C;C) |
| Make rs687289(C;T) |
| Make rs687289(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 9 |
| Position | 133261703 |
| Gene | ABO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs687289 |
| dbSNP (classic) | rs687289 |
| ClinGen | rs687289 |
| ebi | rs687289 |
| HLI | rs687289 |
| Exac | rs687289 |
| Gnomad | rs687289 |
| Varsome | rs687289 |
| LitVar | rs687289 |
| Map | rs687289 |
| PheGenI | rs687289 |
| Biobank | rs687289 |
| 1000 genomes | rs687289 |
| hgdp | rs687289 |
| ensembl | rs687289 |
| geneview | rs687289 |
| scholar | rs687289 |
| rs687289 | |
| pharmgkb | rs687289 |
| gwascentral | rs687289 |
| openSNP | rs687289 |
| 23andMe | rs687289 |
| SNPshot | rs687289 |
| SNPdbe | rs687289 |
| MSV3d | rs687289 |
| GWAS Ctlg | rs687289 |
| GMAF | 0.3673 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23267103 ]
|
| Trait | Coagulation factor levels |
| Title | Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association. |
| Risk Allele | T |
| P-val | 1E-128 |
| Odds Ratio | .33 [0.30-0.36] lU/dL increase |
[PMID 18604267] Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.
| GWAS snp | |
|---|---|
| PMID | [PMID 24586186]
|
| Trait | Urinary metabolites (H-NMR features) |
| Title | Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links. |
| Risk Allele | G |
| P-val | 1E-12 |
| Odds Ratio | .27 [NR] unit increase |
