{{Rsnum
|rsid=121908840
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TP63
|position=189867903
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TP63
}}{{omim
|id=603273
|rsnum=121908840
|variant=0007
}}{{ClinVar
|rsid=121908840
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=189585692
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TP63:8626
|GENE_NAME=TP63
|GENE_ID=8626
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.189585692G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603273.0007
|CLNSIG=5
|CLNCUI=C1858562; C1785148
|CLNDBN=Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3; Rapp-Hodgkin ectodermal dysplasia syndrome
|Disease=Ectrodactyly; Rapp-Hodgkin ectodermal dysplasia syndrome
|CLNACC=RCV000006906.1; RCV000006907.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C1858562:604292:1896; C1785148:129400:7731005
}}