{{Rsnum
|rsid=267607353
|Chromosome=12
|position=6016197
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=VWF
|Gene_s=VWF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=C
|CHROM=12
|CLNACC=RCV000024004.1; RCV000086836.1
|CLNALLE=1
|CLNDBN=von Willebrand disease type 2; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK7014:C1264040:613554:166081:903:128107007
|CLNHGVS=NC_000012.11:g.6125363A>C
|CLNSIG=5
|CLNSRC=Academic Unit of Haematology; OMIM Allelic Variant
|CLNSRCID=VWF_5347; 613160.0042
|Disease=von Willebrand disease type 2; not provided
|FwdALT=G
|FwdREF=T
|GENEINFO=VWF:7450
|GENE_ID=7450
|GENE_NAME=VWF
|REF=A
|RSPOS=6125363
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050360000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=267607353
}}