{{Rsnum
|rsid=121964895
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VWF
|position=6021960
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VWF
}}{{omim
|id=613160
|rsnum=121964895
|variant=0027
}}{{ClinVar
|rsid=121964895
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=6131126
|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; 2
|CLNHGVS=NC_000012.11:g.6131126C>A; NC_000012.11:g.6131126C>T
|CLNSRC=Academic Unit of Haematology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=VWF_3614__1; VWF_3614; 613160.0027
|CLNSIG=5
|CLNCUI=C1264039
|CLNDBN=not provided; von Willebrand disease type 1; von Willebrand factor Vicenza
|Disease=not provided; von Willebrand disease type 1; von Willebrand factor Vicenza
|CLNACC=RCV000086667.1; RCV000000335.1; RCV000000336.1; RCV000086666.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK7014:C1264039:193400:166078:903:128106003
}}