{{Rsnum
|rsid=111033554
|Chromosome=6
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COL10A1
|position=116120326
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COL10A1,NT5DC1
}}{{omim
|id=120110
|rsnum=111033554
|variant=0017
}}{{ClinVar
|rsid=111033554
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=116441489
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=NT5DC1:221294; COL10A1:1300
|GENE_NAME=NT5DC1; COL10A1
|GENE_ID=221294; 1300
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.116441489T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120110.0017
|CLNSIG=5
|CLNCUI=C0265289
|CLNDBN=Metaphyseal chondrodysplasia, Schmid type
|Disease=Metaphyseal chondrodysplasia
|CLNACC=RCV000019032.26
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265289:156500:174:29248006
}}{{PMID Auto
|PMID=9852679
|Title=Novel missense mutation resulting in the substitution of tyrosine by cysteine at codon 597 of the type X collagen gene associated with Schmid metaphyseal chondrodysplasia.
}}