{{Rsnum
|rsid = 28928897
|Gene = KRT17
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=C
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=17
|position=41624229
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT17
}}{{omim
|desc=STEATOCYSTOMA MULTIPLEX
|id=148069
|rsnum=28928897
|variant=0005
}}
{{omim
|desc=PACHYONYCHIA CONGENITA, TYPE 2
|id=148069
|rsnum=28928897
|variant=0009
}}
{{ neighbor
| rsid = 28928899
| distance = 3
}}
{{ neighbor
| rsid = 28928896
| distance = 7
}}{{ClinVar
|rsid=28928897
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=39780481
|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; 2
|CLNHGVS=NC_000017.10:g.39780481C>G; NC_000017.10:g.39780481C>T
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT17:c.281G>C; 148069.0009; KRT17:c.281G>A; 148069.0005
|CLNCUI=C1721007,C0259771; C1721007
|CLNDBN=Pachyonychia congenita type 2; not provided; Steatocystoma multiplex
|Disease=Pachyonychia congenita type 2; not provided; Steatocystoma multiplex
|CLNACC=RCV000015698.20; RCV000056516.1; RCV000015692.24; RCV000015693.24; RCV000056515.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1280:C1721007:167210:2309; C0259771:184500:841:109433009
|CLNSIG=5
}}