{{Rsnum
|rsid=121908845
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TP63
|position=189889478
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TP63
}}{{omim
|id=603273
|rsnum=121908845
|variant=0018
}}{{ClinVar
|rsid=121908845
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=189607267
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TP63:8626
|GENE_NAME=TP63
|GENE_ID=8626
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.189607267T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603273.0018
|CLNSIG=5
|CLNCUI=C0406709; C1785148
|CLNDBN=Hay-Wells syndrome of ectodermal dysplasia; Rapp-Hodgkin ectodermal dysplasia syndrome
|Disease=Hay-Wells syndrome of ectodermal dysplasia; Rapp-Hodgkin ectodermal dysplasia syndrome
|CLNACC=RCV000006918.1; RCV000006919.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK43797:C0406709:106260:1071:55821006; C1785148:129400:7731005
}}