{{Rsnum
|rsid = 28928893
|Gene = KRT14
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=17
|position=41586479
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT14
}}{{omim
|desc=EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE
|id=148066
|rsnum=28928893
|variant=0009
}}

{{ neighbor
| rsid = 3826550
| distance = 76
}}

{{ClinVar
|rsid=28928893
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=39742731
|CHROM=17
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=KRT14:3861
|GENE_NAME=KRT14
|GENE_ID=3861
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.39742731A>G
|CLNSRC=Epithelial Biology; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT14:c.356T>C; NBK1369; 148066.0009
|CLNSIG=5
|CLNCUI=C0079295; C0079295
|CLNDBN=Epidermolysis bullosa herpetiformis, Dowling-Meara; not provided
|Disease=Epidermolysis bullosa herpetiformis; not provided
|CLNACC=RCV000015723.24; RCV000056708.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1369:C0079295:131760:79396
}}

{{PMID Auto
|PMID=9804355
|Title=Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14).
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}