{{Rsnum
|rsid=386833986
|Chromosome=12
|position=91055447
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KERA
|Gene_s=KERA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=A
|CHROM=12
|CLNACC=RCV000049963.1
|CLNALLE=1
|CLNDBN=Cornea plana 2
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1857574:217300
|CLNHGVS=NC_000012.11:g.91449224G>A
|CLNSIG=4
|Disease=Cornea plana 2
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=91449224
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833986
|GENEINFO=KERA:11081
|GENE_ID=11081
|GENE_NAME=KERA
}}{{PMID Auto
|PMID=16234475
|Title=Pellucid marginal degeneration coexistent with cornea plana in one member of a family exhibiting a novel KERA mutation.
|OA=1
}}