{{Rsnum
|rsid=121908616
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CHST3
|position=72007807
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CHST3
}}{{omim
|id=603799
|rsnum=121908616
|variant=0002
}}{{ClinVar
|rsid=121908616
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=73767565
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CHST3:9469
|GENE_NAME=CHST3
|GENE_ID=9469
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.73767565T>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000006413.1
|CLNDBN=Spondyloepiphyseal dysplasia with congenital joint dislocations
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:OMIM:Orphanet
|CLNDSDBID=NBK1129:NBK62112:C1840471:143095:608637:263463
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603799.0002
|Disease=Spondyloepiphyseal dysplasia with congenital joint dislocations
}}