{{Rsnum
|rsid = 28928896
|Gene = KRT17
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=C
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=17
|position=41624236
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT17
}}{{omim
|desc=STEATOCYSTOMA MULTIPLEX
|id=148069
|rsnum=28928896
|variant=0004
}}

During some blast and clustalw analysis of the watson genome, this snp is an outlier. It appears to occur in a fairly well conserved region, which appears slightly differently at several places in the genome.
{{ neighbor
| rsid = 28928897
| distance = 7
}}
{{ neighbor
| rsid = 28928898
| distance = 11
}}

{{omim
|id=148069
|rsnum=28928896
|variant=0001
}}

{{ClinVar
|rsid=28928896
|Reversed=1
|FwdREF=A
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=39780488
|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.39780488T>C; NC_000017.10:g.39780488T>G
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT17:c.274A>G; 148069.0001; KRT17:c.274A>C; 148069.0004
|CLNSIG=5
|CLNCUI=C1721007; C0259771
|CLNDBN=Pachyonychia congenita type 2; not provided; Steatocystoma multiplex
|Disease=Pachyonychia congenita type 2; not provided; Steatocystoma multiplex
|CLNACC=RCV000015688.25; RCV000056510.1; RCV000015691.24; RCV000056509.1
|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
}}

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