{{Rsnum
|rsid=62643630
|Chromosome=12
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=VWF
|Gene_s=VWF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=6044322
}}{{ClinVar
|ALT=A
|CHROM=12
|CLNACC=RCV000000341.1; RCV000086609.1
|CLNALLE=1
|CLNDBN=von Willebrand disease type 2N; not provided
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C1282975:359732009
|CLNHGVS=NC_000012.11:g.6153488C>A
|CLNSIG=5
|CLNSRC=Academic Unit of Haematology; OMIM Allelic Variant
|CLNSRCID=VWF_2411; 613160.0032
|Disease=von Willebrand disease type 2N; not provided
|FwdALT=T
|FwdREF=G
|GENEINFO=VWF:7450
|GENE_ID=7450
|GENE_NAME=VWF
|REF=C
|RSPOS=6153488
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050160000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=62643630
}}