{{Rsnum
|rsid=60627726
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KRT6B
|position=52447788
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KRT6B
}}{{omim
|id=148042
|rsnum=60627726
|variant=0001
}}

{{ClinVar
|rsid=60627726
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=52841572
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=KRT6B:3854
|GENE_NAME=KRT6B
|GENE_ID=3854
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.52841572C>T
|CLNSRC=Epithelial Biology; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=KRT6B:c.1414G>A; 148042.0001
|CLNSIG=5
|CLNCUI=C1721007
|CLNDBN=Pachyonychia congenita type 2; not provided
|Disease=Pachyonychia congenita type 2; not provided
|CLNACC=RCV000015739.20; RCV000057023.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1280:C1721007:167210:2309
}}

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