{{Rsnum
|rsid=80356555
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=VCAN
|position=83537005
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VCAN
}}{{omim
|id=118661
|rsnum=80356555
|variant=0001
}}{{ClinVar
|rsid=80356555
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=82832824
|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
|CLNHGVS=NC_000005.9:g.82832824A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK3821; 118661.0001
|CLNSIG=5
|CLNCUI=C0339540; C0339540
|CLNDBN=Wagner syndrome
|Disease=Wagner syndrome
|CLNACC=RCV000019046.27
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK3821:C0339540:143200:898:232064001
}}{{PMID|16043844}} Identification of a novel splice site mutation of the CSPG2 gene in a Japanese family with Wagner syndrome.

{{PMID|16877430}} Erosive vitreoretinopathy and wagner disease are caused by intronic mutations in CSPG2/Versican that result in an imbalance of splice variants.