{{Rsnum
|rsid=121908477
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ADAMTS13
|position=133428750
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ADAMTS13
}}{{omim
|id=604134
|rsnum=121908477
|variant=0014
}}{{ClinVar
|ALT=C
|CHROM=9
|CLNACC=RCV000006168.1
|CLNALLE=1
|CLNDBN=Upshaw-Schulman syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1268935:274150:54057:373420004
|CLNHGVS=NC_000009.11:g.136293870G>C
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604134.0014
|Disease=Upshaw-Schulman syndrome
|FwdALT=C
|FwdREF=G
|GENEINFO=ADAMTS13:11093
|GENE_ID=11093
|GENE_NAME=ADAMTS13
|REF=G
|RSPOS=136293870
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=121908477
}}