{{Rsnum
|rsid=10510829
|Gene=FHIT
|Chromosome=3
|position=60137795
|Orientation=plus
|GMAF=0.1437
|Gene_s=FHIT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 58.0 | 33.9 | 8.0
| HCB | 70.1 | 29.2 | 0.7
| JPT | 85.0 | 15.0 | 0.0
| YRI | 95.9 | 4.1 | 0.0
| ASW | 82.5 | 15.8 | 1.8
| CHB | 70.1 | 29.2 | 0.7
| CHD | 81.5 | 15.7 | 2.8
| GIH | 61.0 | 29.0 | 10.0
| LWK | 89.0 | 11.0 | 0.0
| MEX | 75.4 | 24.6 | 0.0
| MKK | 83.3 | 16.7 | 0.0
| TSI | 59.8 | 37.3 | 2.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22379998
|Trait=None
|Title=Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.
|RiskAllele=
|Pval=7E-7
|OR=None
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}