{{Rsnum
|rsid=1800382
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VWF
|position=6019222
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VWF
}}{{omim
|id=613160
|rsnum=1800382
|variant=0010
}}{{ClinVar
|rsid=1800382
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=6128388
|CHROM=12
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050160000000040002110100
|GENEINFO=VWF:7450
|GENE_NAME=VWF
|GENE_ID=7450
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.6128388C>T
|CLNORIGIN=1
|CLNSIG=2
|Tags=RV;PM;SLO;VLD;OTHERKG;LSD;OM
|CLNACC=RCV000000317.1
|CLNDBN=VON WILLEBRAND FACTOR POLYMORPHISM
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613160.0010
|Disease=VON WILLEBRAND FACTOR POLYMORPHISM
}}