{{Rsnum
|rsid=61749403
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VWF
|position=6019396
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VWF
}}{{omim
|id=613160
|rsnum=61749403
|variant=0008
}}

{{ClinVar
|rsid=61749403
|Reversed=1
|FwdREF=G
|FwdALT=A,C,T
|REF=C
|ALT=A,G,T
|RSPOS=6128562
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110104
|GENEINFO=VWF:7450
|GENE_NAME=VWF
|GENE_ID=7450
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000012.11:g.6128562C>A; NC_000012.11:g.6128562C>G; NC_000012.11:g.6128562C>T
|CLNSRC=Academic Unit of Haematology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=VWF_4022__2; VWF_4022__1; VWF_4022; 613160.0008
|CLNSIG=5
|CLNCUI=C1282971
|CLNDBN=not provided; von Willebrand disease, type 2b
|Disease=not provided; von Willebrand disease
|CLNACC=RCV000086723.1; RCV000086722.1; RCV000000315.1; RCV000086721.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDSDB=MedGen
|CLNDSDBID=C1282971
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}