{{Rsnum
|rsid=723524
|Gene=CTNNA2
|Chromosome=2
|position=80354676
|Orientation=plus
|GMAF=0.2066
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=CTNNA2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 60.7 | 37.5 | 1.8
| HCB | 40.4 | 45.6 | 14.0
| JPT | 33.6 | 47.8 | 18.6
| YRI | 94.6 | 5.4 | 0.0
| ASW | 96.5 | 3.5 | 0.0
| CHB | 40.4 | 45.6 | 14.0
| CHD | 45.9 | 45.9 | 8.3
| GIH | 72.3 | 25.7 | 2.0
| LWK | 97.3 | 2.7 | 0.0
| MEX | 46.3 | 48.1 | 5.6
| MKK | 96.1 | 3.9 | 0.0
| TSI | 70.7 | 25.3 | 4.0
| HapMapRevision=28
}}

{{PMID|17667961|OA=1
}} having minor alleles at all 3 of [[rs1446109]]-[[rs1007371]]-[[rs723524]] may affect [[left]]-right asymmetrical brain function, such as handedness, and much of human cognition, behavior and emotion. [https://genepi.qimr.edu.au/contents/p/staff/CV522.pdf pdf full paper]

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}