{{Rsnum
|rsid=57358989
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KRT14
|position=41586478
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT14
}}{{omim
|id=148066
|rsnum=57358989
|variant=0010
}}

{{ClinVar
|rsid=57358989
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=39742730
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=KRT14:3861
|GENE_NAME=KRT14
|GENE_ID=3861
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.39742730C>T
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT14:c.357G>A; 148066.0010
|CLNSIG=5
|CLNCUI=C0080333; C1832926
|CLNDBN=Epidermolysis bullosa simplex, Cockayne-Touraine type; Epidermolysis bullosa simplex, autosomal recessive; not provided
|Disease=Epidermolysis bullosa simplex; Epidermolysis bullosa simplex; not provided
|CLNACC=RCV000015724.24; RCV000056256.24; RCV000056709.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1369:C0080333:131800:79400; NBK1369:C1832926:601001:89838
}}

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