{{Rsnum
|rsid = 28933088
|Gene = KRT17
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=G
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=17
|position=41624218
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT17
}}{{omim
|desc=PACHYONYCHIA CONGENITA, TYPE 2
|id=148069
|rsnum=28933088
|variant=0003
}}
{{ neighbor
| rsid = 28933089
| distance = 4
}}
{{ neighbor
| rsid = 28928899
| distance = 8
}}

{{ClinVar
|rsid=28933088
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=39780470
|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.39780470A>C
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT17:c.292T>G; 148069.0003
|CLNSIG=5
|CLNCUI=C1721007
|CLNDBN=Pachyonychia congenita type 2; not provided
|Disease=Pachyonychia congenita type 2; not provided
|CLNACC=RCV000015690.20; RCV000056521.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1280:C1721007:167210:2309
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}