{{Rsnum
|rsid=121908471
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ADAMTS13
|position=133433478
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ADAMTS13
}}{{omim
|id=604134
|rsnum=121908471
|variant=0005
}}{{ClinVar
|ALT=A
|CHROM=9
|CLNACC=RCV000006158.1; RCV000068570.2
|CLNALLE=1
|CLNDBN=Upshaw-Schulman syndrome; Malignant melanoma
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:SNOMED_CT
|CLNDSDBID=C1268935:274150:54057:373420004; C0025202:2092003
|CLNHGVS=NC_000009.11:g.136298598G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604134.0005
|Disease=Upshaw-Schulman syndrome; Malignant melanoma
|FwdALT=A
|FwdREF=G
|GENEINFO=ADAMTS13:11093
|GENE_ID=11093
|GENE_NAME=ADAMTS13
|REF=G
|RSPOS=136298598
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=121908471
}}