{{Rsnum
|rsid=10510837
|Gene=FHIT
|Chromosome=3
|position=60304113
|Orientation=plus
|GMAF=0.09688
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=FHIT
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 29.2 | 70.8
| HCB | 1.5 | 14.6 | 83.9
| JPT | 0.0 | 5.3 | 94.7
| YRI | 0.7 | 10.9 | 88.4
| ASW | 1.8 | 14.0 | 84.2
| CHB | 1.5 | 14.6 | 83.9
| CHD | 0.9 | 10.1 | 89.0
| GIH | 0.0 | 18.8 | 81.2
| LWK | 0.9 | 8.2 | 90.9
| MEX | 1.8 | 24.6 | 73.7
| MKK | 0.0 | 10.9 | 89.1
| TSI | 2.0 | 17.8 | 80.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21182207
|Trait=None
|Title=Variants in several genomic regions associated with Asperger disorder
|RiskAllele=
|Pval=0.000004
|OR=None
|ORtxt=None
}}

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