{{Rsnum
|rsid = 28928895
|Gene = KRT16
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Chromosome=17
|position=41612306
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT16
}}This SNP has been found in patients with [[pachyonychia congenita Type I]], and the risk allele appears to be a causative mutation for this (dominant) disorder.
See also: [http://www.ncbi.nlm.nih.gov/omim/148067?db=omim&dopt=Detailed#148067Variants001 OMIM 148067.0010]

{{ neighbor
| rsid = 28928894
| distance = 21
}}

{{omim
|id=148067
|rsnum=28928895
|variant=0010
}}

{{ClinVar
|rsid=28928895
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=39768558
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=KRT16:3868
|GENE_NAME=KRT16
|GENE_ID=3868
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.39768558A>T
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT16:c.383T>A; 148067.0010
|CLNSIG=5
|CLNCUI=C1706595
|CLNDBN=Pachyonychia congenita, type 1; not provided
|Disease=Pachyonychia congenita; not provided
|CLNACC=RCV000015713.20; RCV000057040.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1280:C1706595:167200:2309
}}

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