{{Rsnum
|rsid=28936368
|Gene=COMP
|Chromosome=19
|position=18783129
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.001837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=COMP
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 96.1 | 3.9 | 0.0
| HapMapRevision=28
}}

{{omim
|desc=EPIPHYSEAL DYSPLASIA, MULTIPLE, FAIRBANK TYPE
|id=600310
|rsnum=28936368
|variant=0017
}}

{{ClinVar
|rsid=28936368
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=18893939
|CHROM=19
|GMAF=0.0018
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000416110100
|GENEINFO=COMP:1311
|GENE_NAME=COMP
|GENE_ID=1311
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.18893939G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1123; 600310.0017
|CLNSIG=5
|CLNCUI=C1838280
|CLNDBN=Multiple epiphyseal dysplasia 1
|Disease=Multiple epiphyseal dysplasia 1
|CLNACC=RCV000009776.2
|Tags=RV;PM;S3D;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9982; 0.001837
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1123:C1838280:132400
|COMMON=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}