{{Rsnum
|rsid=121908473
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ADAMTS13
|position=133437895
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ADAMTS13
}}{{omim
|id=604134
|rsnum=121908473
|variant=0007
}}{{ClinVar
|ALT=G
|CHROM=9
|CLNACC=RCV000006160.1
|CLNALLE=1
|CLNDBN=Upshaw-Schulman syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1268935:274150:54057:373420004
|CLNHGVS=NC_000009.11:g.136303015A>G
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604134.0007
|Disease=Upshaw-Schulman syndrome
|FwdALT=G
|FwdREF=A
|GENEINFO=ADAMTS13:11093
|GENE_ID=11093
|GENE_NAME=ADAMTS13
|REF=A
|RSPOS=136303015
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=121908473
}}