{{Rsnum
|rsid=121912478
|Chromosome=17
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TCC)
|geno3=(TCC;TCC)
|Gene=KRT17
|position=41624219
|Gene_s=KRT17
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=148069
|rsnum=121912478
|variant=0012
}}{{ClinVar
|rsid=121912478
|Reversed=1
|FwdREF=CCT
|FwdALT=
|REF=AGGA
|ALT=A
|RSPOS=39780470
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110200
|GENEINFO=KRT17:3872
|GENE_NAME=KRT17
|GENE_ID=3872
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.39780471_39780473delGGA
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT17:c.289_291delTCC; 148069.0012
|CLNSIG=5
|CLNCUI=C1721007
|CLNDBN=Pachyonychia congenita type 2; not provided
|Disease=Pachyonychia congenita type 2; not provided
|CLNACC=RCV000015701.24; RCV000056520.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1280:C1721007:167210:2309
}}