{{Rsnum
|rsid=80338741
|Chromosome=12
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=DCN
|position=91146171
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DCN
}}{{omim
|id=125255
|rsnum=80338741
|variant=0001
}}{{ClinVar
|rsid=80338741
|Reversed=1
|FwdREF=T
|FwdALT=
|REF=GA
|ALT=G
|RSPOS=91539947
|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.91539948delA
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK2690; 125255.0001
|CLNSIG=5
|CLNCUI=C1864738; C1864738
|CLNDBN=Congenital Stromal Corneal Dystrophy
|Disease=Congenital Stromal Corneal Dystrophy
|CLNACC=RCV000018366.26
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK2690:C1864738:610048:101068
}}{{PMID|5304426}} Dystrophia corneae parenchymatosa congenita. A clinical, morphological and histochemical examination.

{{PMID|15671264}} Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene.