{{Rsnum
|rsid=6872664
|Gene=PITX1
|Chromosome=5
|position=135031908
|Orientation=plus
|GMAF=0.1598
|Gene_s=LOC100996485,PITX1
|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 | 87.7 | 10.5 | 1.8
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}mentioned by [[gs240]]{{PMID|18053270|OA=1
}} Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.

{{PMID|20678243|OA=1
}} Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.
{{PMID Auto
|PMID=22739633
|Title=The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families
}}