{{Rsnum
|rsid=58730926
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KRT17
|position=41624230
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT17
}}{{omim
|id=148069
|rsnum=58730926
|variant=0006
}}

{{ClinVar
|rsid=58730926
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=39780482
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=KRT17:3872
|GENE_NAME=KRT17
|GENE_ID=3872
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.39780482G>A
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT17:c.280C>T; 148069.0006
|CLNSIG=5
|CLNCUI=C0259771; C1721007
|CLNDBN=Steatocystoma multiplex; Pachyonychia congenita type 2; not provided
|Disease=Steatocystoma multiplex; Pachyonychia congenita type 2; not provided
|CLNACC=RCV000015694.24; RCV000015695.20; RCV000056513.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C0259771:184500:841:109433009; NBK1280:C1721007:167210:2309
}}

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