{{Rsnum
|rsid=61748478
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VWF
|position=6044349
|Gene_s=VWF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=61748478
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=6153515
|CHROM=12
|dbSNPBuildID=137
|SSR=0
|SAO=0
|VP=0x050160000000000002110100
|GENEINFO=VWF:7450
|GENE_NAME=VWF
|GENE_ID=7450
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.6153515T>C
|CLNSRC=Academic Unit of Haematology; OMIM Allelic Variant
|CLNSRCID=VWF_2384; 613160.0031
|CLNSIG=5
|CLNCUI=C1282975
|CLNDBN=von Willebrand disease type 2N; not provided
|Disease=von Willebrand disease type 2N; not provided
|CLNACC=RCV000000340.1; RCV000086607.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C1282975:359732009
}}

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