{{Rsnum
|rsid=121434224
|Chromosome=1
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=IRF6
|position=209796453
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=IRF6
}}{{omim
|id=607199
|rsnum=121434224
|variant=0001
}}{{ClinVar
|rsid=121434224
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=209796453
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060400605000002110100
|GENEINFO=IRF6:3664
|GENE_NAME=IRF6
|GENE_ID=3664
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.209796453C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001206696.1:c.-12G>T; NM_006147.3:c.274G>T; 607199.0001
|CLNSIG=5
|CLNCUI=C0175697
|CLNDBN=Van der Woude syndrome
|Disease=Van der Woude syndrome
|CLNACC=RCV000003580.1
|Tags=RV;PM;NSN;REF;U5;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1407:C0175697:119300:ORPHA888:79261008
}}