{{Rsnum
|rsid=1063857
|Gene=VWF
|Chromosome=12
|position=6044348
|Orientation=minus
|GMAF=0.3434
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=VWF
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 11.5 | 46.0 | 42.5
| HCB | 0.7 | 10.2 | 89.1
| JPT | 0.9 | 14.2 | 85.0
| YRI | 46.3 | 40.1 | 13.6
| ASW | 36.8 | 49.1 | 14.0
| CHB | 0.7 | 10.2 | 89.1
| CHD | 0.9 | 13.8 | 85.3
| GIH | 4.0 | 28.7 | 67.3
| LWK | 42.7 | 42.7 | 14.5
| MEX | 3.4 | 36.2 | 60.3
| MKK | 24.5 | 45.8 | 29.7
| TSI | 14.7 | 43.1 | 42.2
| 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
}}

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