{{Rsnum
|rsid=137852655
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COMP
|position=18783125
|Gene_s=COMP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600310
|variant=0013
|rsnum=137852655
}}{{ClinVar
|rsid=137852655
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=18893935
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=COMP:1311
|GENE_NAME=COMP
|GENE_ID=1311
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.18893935C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000009772.1; RCV000033890.2
|CLNDBN=Pseudoachondroplasia, severe; Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1487:C0410538:177170:750:22567005
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1487; 600310.0013
|Disease=Pseudoachondroplasia; Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
}}