{{Rsnum
|rsid=212016
|Gene=FHIT
|Chromosome=3
|position=59995799
|Orientation=plus
|GMAF=0.3485
|Gene_s=FHIT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 38.9 | 53.1
| HCB | 16.8 | 46.0 | 37.2
| JPT | 20.4 | 38.1 | 41.6
| YRI | 25.3 | 44.5 | 30.1
| ASW | 21.4 | 53.6 | 25.0
| CHB | 16.8 | 46.0 | 37.2
| CHD | 14.7 | 48.6 | 36.7
| GIH | 23.8 | 42.6 | 33.7
| LWK | 17.4 | 56.9 | 25.7
| MEX | 12.1 | 37.9 | 50.0
| MKK | 23.1 | 51.3 | 25.6
| TSI | 4.9 | 32.4 | 62.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22419666
|Trait=None
|Title=Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.
|RiskAllele=
|Pval=0.000007
|OR=1.5400
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}