{{Rsnum
|rsid=216293
|Gene=VWF
|Chromosome=12
|position=6044493
|Orientation=plus
|GMAF=0.472
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=VWF
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 21.2 | 52.2 | 26.5
| HCB | 5.8 | 43.1 | 51.1
| JPT | 13.4 | 43.8 | 42.9
| YRI | 60.3 | 32.9 | 6.8
| ASW | 60.7 | 35.7 | 3.6
| CHB | 5.8 | 43.1 | 51.1
| CHD | 3.7 | 42.2 | 54.1
| GIH | 8.9 | 39.6 | 51.5
| LWK | 56.4 | 35.5 | 8.2
| MEX | 6.9 | 53.4 | 39.7
| MKK | 29.8 | 47.7 | 22.5
| TSI | 17.6 | 51.0 | 31.4
| 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=22875612
|Title=A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}