{{Rsnum
|rsid=35678
|Gene=ATP2B2
|Chromosome=3
|position=10338239
|Orientation=plus
|GMAF=0.4734
|Gene_s=ATP2B2
|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 | 29.2 | 52.2 | 18.6
| HCB | 19.7 | 51.8 | 28.5
| JPT | 15.2 | 43.8 | 41.1
| YRI | 21.1 | 44.9 | 34.0
| ASW | 17.5 | 40.4 | 42.1
| CHB | 19.7 | 51.8 | 28.5
| CHD | 24.8 | 49.5 | 25.7
| GIH | 9.9 | 49.5 | 40.6
| LWK | 11.8 | 55.5 | 32.7
| MEX | 10.5 | 52.6 | 36.8
| MKK | 9.6 | 46.8 | 43.6
| TSI | 32.4 | 50.0 | 17.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=22739633
|Title=The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families
}}

{{PMID Auto
|PMID=20678243
|Title=Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.
|OA=1
}}

{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}