{{Rsnum
|rsid=387906339
|Chromosome=1
|position=186313753
|Orientation=plus
|geno1=(AG;AG)
|geno2=(AG;CC)
|geno3=(CC;CC)
|Gene=PRG4
|Gene_s=PRG4,TPR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TAG
|CHROM=1
|CLNACC=RCV000006009.1
|CLNALLE=1
|CLNDBN=Camptodactyly arthropathy coxa vara pericarditis syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1859690:208250:ORPHA2848
|CLNHGVS=NC_000001.11:g.186313753_186313754delCCinsAG
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_003292.2:c.*217_*218delGGinsCT; NM_005807.3:c.4190_4191delCCinsAG; 604283.0005
|Disease=Camptodactyly arthropathy coxa vara pericarditis syndrome
|FwdALT=AG
|FwdREF=CC
|REF=TCC
|RSPOS=186313752
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSN;REF;U3;R3;ASP;OTHERKG;LSD;OM
|VC=MNV
|VP=0x050060840605000002110800
|WGT=1
|dbSNPBuildID=137
|rsid=387906339
|GENEINFO=PRG4:10216; TPR:7175
|GENE_ID=10216; 7175
|GENE_NAME=PRG4; TPR
|CLNORIGIN=1
}}