{{Rsnum
|rsid = 28934879
|Gene = VWF
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=12
|position=6021960
|Gene_s=VWF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=121964895
}}{{omim
| id = 193400
| variant = 0027
| desc    = VON WILLEBRAND DISEASE, TYPE IIM
| rsnum   = 28934879
}}