{{Rsnum
|rsid=80356556
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VCAN
|position=83537002
|Gene_s=VCAN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356556
|Reversed=0
|FwdREF=T
|FwdALT=A,C
|REF=T
|ALT=A,C
|RSPOS=82832821
|CHROM=5
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=VCAN:1462
|GENE_NAME=VCAN
|GENE_ID=1462
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000005.9:g.82832821T>A; NC_000005.9:g.82832821T>C
|CLNORIGIN=0
|CLNSRCID=
NBK3821; 118661.0004; 118661.0003
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000020592.2; RCV000020593.2
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDBN=Wagner syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK3821:C0339540:143200:898:232064001
|CLNSRC=GeneReviews; OMIM Allelic Variant
|Disease=Wagner syndrome
}}{{PMID Auto
|PMID=16877430
|Title=Erosive vitreoretinopathy and wagner disease are caused by intronic mutations in CSPG2/Versican that result in an imbalance of splice variants.
}}