{{Rsnum
|rsid=121434357
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ADAMTS10
|position=8601029
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ADAMTS10
}}{{omim
|id=608990
|rsnum=121434357
|variant=0001
}}{{ClinVar
|rsid=121434357
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=8665913
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ADAMTS10:81794
|GENE_NAME=ADAMTS10
|GENE_ID=81794
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.8665913G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608990.0001
|CLNSIG=5
|CLNCUI=C1869114
|CLNDBN=Weill-Marchesani syndrome 1
|Disease=Weill-Marchesani syndrome 1
|CLNACC=RCV000002021.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1114:C1869114:277600:3449
}}