{{Rsnum
|rsid=58751565
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=KRT5
|position=52520283
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT5
}}{{omim
|id=148040
|rsnum=58751565
|variant=0019
}}{{ClinVar
|rsid=58751565
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=52914067
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=KRT5:3852
|GENE_NAME=KRT5
|GENE_ID=3852
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.52914067G>T
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT5:c.14C>A; 148040.0019
|CLNSIG=5
|CLNCUI=C0406811
|CLNDBN=Reticulate acropigmentation of Kitamura; not provided
|Disease=Reticulate acropigmentation of Kitamura; not provided
|CLNACC=RCV000015753.22; RCV000056572.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0406811:179850:79145:239133004
}}