{{Rsnum
|rsid=121908470
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ADAMTS13
|position=133426246
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ADAMTS13
}}{{omim
|id=604134
|rsnum=121908470
|variant=0004
}}{{ClinVar
|ALT=T
|CHROM=9
|CLNACC=RCV000006157.1
|CLNALLE=1
|CLNDBN=Upshaw-Schulman syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1268935:274150:54057:373420004
|CLNHGVS=NC_000009.11:g.136291366C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604134.0004
|Disease=Upshaw-Schulman syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=ADAMTS13:11093
|GENE_ID=11093
|GENE_NAME=ADAMTS13
|REF=C
|RSPOS=136291366
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=121908470
}}