{{Rsnum
|rsid=61748511
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VWF
|position=6022833
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VWF
}}{{omim
|id=613160
|rsnum=61748511
|variant=0028
}}{{ClinVar
|rsid=61748511
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=6131999
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=VWF:7450
|GENE_NAME=VWF
|GENE_ID=7450
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.6131999A>G
|CLNSRC=Academic Unit of Haematology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=VWF_3445; 613160.0028
|CLNSIG=5
|CLNCUI=C1264039
|CLNDBN=von Willebrand disease type 1; not provided
|Disease=von Willebrand disease type 1; not provided
|CLNACC=RCV000000337.1; RCV000086657.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK7014:C1264039:193400:166078:903:128106003
}}