{{Rsnum
|rsid=479632
|Gene=PITX1
|Chromosome=5
|position=135028828
|Orientation=minus
|GMAF=0.3182
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=PITX1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 7.9 | 42.9 | 49.2
| HCB | 26.7 | 48.9 | 24.4
| JPT | 38.6 | 43.2 | 18.2
| YRI | 3.2 | 21.0 | 75.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 26.7 | 48.9 | 24.4
| 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
}}{{PMID Auto
|PMID=20054692
|Title=Genetic polymorphism of PITX1 in susceptibility to knee osteoarthritis in a Chinese Han population: a case-control study
}}

{{PMID Auto
|PMID=18053270
|Title=Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.
|OA=1
}}

{{GET Evidence
|gene=PITX1
|aa_change=Gly299Ala
|aa_change_short=G299A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs479632
|overall_frequency_n=2319
|overall_frequency_d=10758
|overall_frequency=0.215561
|n_genomes=9
|n_genomes_annotated=0
|n_haplomes=10
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}