{{Rsnum
|rsid=237889
|Gene=OXTR
|Chromosome=3
|position=8760797
|Orientation=plus
|GMAF=0.3191
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=OXTR
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 38.1 | 49.6 | 12.4
| HCB | 34.3 | 46.0 | 19.7
| JPT | 25.0 | 54.5 | 20.5
| YRI | 82.9 | 16.4 | 0.7
| ASW | 71.9 | 24.6 | 3.5
| CHB | 34.3 | 46.0 | 19.7
| CHD | 35.8 | 47.7 | 16.5
| GIH | 34.7 | 50.5 | 14.9
| LWK | 74.5 | 24.5 | 0.9
| MEX | 58.6 | 32.8 | 8.6
| MKK | 68.6 | 26.9 | 4.5
| TSI | 37.6 | 46.5 | 15.8
| HapMapRevision=28
}}
{{PMID Auto
|PMID=17893705
|Title=Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition.
}}

{{PMID Auto
|PMID=17668382
|Title=Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium.
|OA=1
}}

{{PMID Auto
|PMID=19461999
|Title=The oxytocin receptor (OXTR) contributes to prosocial fund allocations in the dictator game and the social value orientations task.
|OA=1
}}

{{PMID Auto
|PMID=21934640
|Title=Test of association between 10 single nucleotide polymorphisms in the oxytocin receptor gene and conduct disorder.
|OA=1
}}

{{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}}