{{Rsnum
|rsid=61749370
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VWF
|Gene_s=VWF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=6019621
}}{{ClinVar
|ALT=A,T
|CHROM=12
|CLNACC=RCV000000342.2; RCV000086676.1; RCV000086675.1
|CLNALLE=1; 2
|CLNDBN=von Willebrand disease, type 2b; not provided
|CLNDSDB=MedGen
|CLNDSDBID=C1282971
|CLNHGVS=NC_000012.11:g.6128787G>A; NC_000012.11:g.6128787G>T
|CLNSIG=5
|CLNSRC=Academic Unit of Haematology; OMIM Allelic Variant
|CLNSRCID=VWF_3797__1; 613160.0033; VWF_3797
|Disease=von Willebrand disease; not provided
|FwdALT=A,T
|FwdREF=C
|GENEINFO=VWF:7450
|GENE_ID=7450
|GENE_NAME=VWF
|REF=G
|RSPOS=6128787
|Reversed=1
|SAO=0
|SSR=1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050160000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=61749370
}}