{{Rsnum
|rsid=2235375
|Gene=IRF6
|Chromosome=1
|position=209792242
|Orientation=plus
|GMAF=0.4045
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=IRF6
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 11.0 | 50.5 | 38.5
| HCB | 31.6 | 51.5 | 16.9
| JPT | 32.7 | 54.0 | 13.3
| YRI | 7.5 | 34.7 | 57.8
| ASW | 12.3 | 47.4 | 40.4
| CHB | 31.6 | 51.5 | 16.9
| CHD | 33.9 | 51.4 | 14.7
| GIH | 22.0 | 52.0 | 26.0
| LWK | 2.8 | 31.2 | 66.1
| MEX | 27.6 | 43.1 | 29.3
| MKK | 12.5 | 43.4 | 44.1
| TSI | 11.8 | 41.2 | 47.1
| HapMapRevision=28
}}

{{omim
|desc=OROFACIAL CLEFT 6, SUSCEPTIBILITY TO; OFC6
|id=608864
|rsnum=2235375
}}

{{PMID Auto
|PMID=19734457
|Title=Association between IRF6 SNPs and oral clefts in West China
|OA=1
}}

{{PMID|15558496|OA=1
}} Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population.

{{PMID|17318851|OA=1
}} Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis.

{{PMID|18278815|OA=1
}} Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway.

{{PMID|20215007|OA=1
}} Genetic control of individual differences in gene-specific methylation in human brain.

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}