{{Rsnum
|rsid=4764478
|Gene=VWF
|Chromosome=12
|position=5968959
|Orientation=plus
|GMAF=0.1763
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=VWF
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 3.5 | 38.9 | 57.5
| HCB | 0.0 | 3.6 | 96.4
| JPT | 0.9 | 10.6 | 88.5
| YRI | 5.5 | 28.1 | 66.4
| ASW | 5.3 | 45.6 | 49.1
| CHB | 0.0 | 3.6 | 96.4
| CHD | 0.0 | 5.5 | 94.5
| GIH | 6.9 | 41.6 | 51.5
| LWK | 12.7 | 31.8 | 55.5
| MEX | 3.4 | 34.5 | 62.1
| MKK | 5.1 | 29.5 | 65.4
| TSI | 7.0 | 39.0 | 54.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20940418
|Title=Variation in the von Willebrand Factor gene is associated with VWF levels and with the risk of cardiovascular disease
}}

{{PMID Auto
|PMID=20346360
|Title=Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease.
|OA=1
}}

{{on chip | Affy GenomeWide 6}}