{{Rsnum
|rsid = 28942093
|Gene = IRF6
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=1
|position=209801409
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=IRF6
}}{{omim
|desc=VAN DER WOUDE SYNDROME
|id=607199
|rsnum=28942093
|variant=0006
}}
{{ neighbor
| rsid = 28942094
| distance = 11
}}{{ClinVar
|rsid=28942093
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=209801409
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060080a05000002110100
|GENEINFO=IRF6:3664
|GENE_NAME=IRF6
|GENE_ID=3664
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.209801409G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001206696.1:c.-112+4538C>T; NM_006147.3:c.5C>T; 607199.0006
|CLNSIG=5
|CLNCUI=C0175697
|CLNDBN=Van der Woude syndrome
|Disease=Van der Woude syndrome
|CLNACC=RCV000003585.1
|Tags=RV;PM;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1407:C0175697:119300:ORPHA888:79261008
}}