rs4764478
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4764478(A;A) |
| Make rs4764478(A;T) |
| Make rs4764478(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 5968959 |
| Gene | VWF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4764478 |
| dbSNP (classic) | rs4764478 |
| ClinGen | rs4764478 |
| ebi | rs4764478 |
| HLI | rs4764478 |
| Exac | rs4764478 |
| Gnomad | rs4764478 |
| Varsome | rs4764478 |
| LitVar | rs4764478 |
| Map | rs4764478 |
| PheGenI | rs4764478 |
| Biobank | rs4764478 |
| 1000 genomes | rs4764478 |
| hgdp | rs4764478 |
| ensembl | rs4764478 |
| geneview | rs4764478 |
| scholar | rs4764478 |
| rs4764478 | |
| pharmgkb | rs4764478 |
| gwascentral | rs4764478 |
| openSNP | rs4764478 |
| 23andMe | rs4764478 |
| SNPshot | rs4764478 |
| SNPdbe | rs4764478 |
| MSV3d | rs4764478 |
| GWAS Ctlg | rs4764478 |
| GMAF | 0.1763 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20940418] Variation in the von Willebrand Factor gene is associated with VWF levels and with the risk of cardiovascular disease
[PMID 20346360
] Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease.
