{{Rsnum
|rsid=80338742
|Chromosome=12
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=DCN
|position=91146197
|Gene_s=DCN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338742
|Reversed=1
|FwdREF=C
|FwdALT=
|REF=TG
|ALT=T
|RSPOS=91539973
|CHROM=12
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=DCN:1634
|GENE_NAME=DCN
|GENE_ID=1634
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.91539974delG
|CLNSRC=GeneReviews
|CLNORIGIN=0
|CLNSRCID=NBK2690
|CLNSIG=5
|CLNCUI=C1864738
|CLNDBN=Congenital Stromal Corneal Dystrophy
|Disease=Congenital Stromal Corneal Dystrophy
|CLNACC=RCV000020465.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK2690:C1864738:610048:101068
}}{{PMID|16935612}} A second decorin frame shift mutation in a family with congenital stromal corneal dystrophy.