{{Rsnum
|rsid = 28937593
|Gene = CHST3
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=10
|position=72007942
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CHST3
}}{{omim
|desc=SPONDYLOEPIPHYSEAL DYSPLASIA, OMANI TYPE
|id=603799
|rsnum=28937593
|variant=0001
}}
{{ neighbor
| rsid = 3740129
| distance = 159
}}

{{ClinVar
|rsid=28937593
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=73767700
|CHROM=10
|dbSNPBuildID=132
|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.73767700G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000006412.1
|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=603799.0001
|Disease=Spondyloepiphyseal dysplasia with congenital joint dislocations
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}