{{Rsnum
|rsid=397515437
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=VCAN
|position=83542270
|Gene_s=VCAN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=5
|CLNACC=RCV000034808.28
|CLNALLE=1
|CLNDBN=Wagner syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK3821:C0339540:143200:898:232064001
|CLNHGVS=NC_000005.9:g.82838089T>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK3821; 118661.0007
|Disease=Wagner syndrome
|FwdALT=A
|FwdREF=T
|GENEINFO=VCAN:1462
|GENE_ID=1462
|GENE_NAME=VCAN
|REF=T
|RSPOS=82838089
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397515437
}}