{{Rsnum
|rsid=281875305
|Chromosome=9
|position=133437836
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ADAMTS13
|Gene_s=ADAMTS13
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=A
|CHROM=9
|CLNACC=RCV000006169.1; RCV000059755.1
|CLNALLE=1
|CLNDBN=Upshaw-Schulman syndrome; not provided
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1268935:274150:54057:373420004
|CLNHGVS=NC_000009.11:g.136302956G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=604134.0015; VAR_027122
|Disease=Upshaw-Schulman syndrome; not provided
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=136302956
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=281875305
|GENEINFO=ADAMTS13:11093
|GENE_ID=11093
|GENE_NAME=ADAMTS13
}}{{PMID Auto
|PMID=12181489
|Title=Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity.
|OA=1
}}