{{Rsnum
|rsid=61749392
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=VWF
|position=6019479
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VWF
}}{{omim
|id=613160
|rsnum=61749392
|variant=0004
}}

{{ClinVar
|rsid=61749392
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=6128645
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=VWF:7450
|GENE_NAME=VWF
|GENE_ID=7450
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.6128645C>G
|CLNSRC=Academic Unit of Haematology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=VWF_3939; 613160.0004
|CLNSIG=5
|CLNCUI=C1282971
|CLNDBN=von Willebrand disease, type 2b; not provided
|Disease=von Willebrand disease; not provided
|CLNACC=RCV000000311.1; RCV000086709.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1282971
}}

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