{{Rsnum
|rsid=397515434
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=IRF6
|position=209801269
|Gene_s=IRF6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000033164.1
|CLNALLE=1
|CLNDBN=Van der Woude syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1407:C0175697:119300:ORPHA888:79261008
|CLNHGVS=NC_000001.11:g.209801269G>A
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_001206696.1:c.-112+4678C>T; NM_006147.3:c.145C>T; 607199.0017
|Disease=Van der Woude syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=IRF6:3664
|GENE_ID=3664
|GENE_NAME=IRF6
|REF=G
|RSPOS=209801269
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSN;REF;INT;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060080605000002110100
|WGT=1
|dbSNPBuildID=136
|rsid=397515434
|CLNORIGIN=1
}}