{{Rsnum
|rsid=4741652
|Gene=SMARCA2
|Chromosome=9
|position=2194227
|Orientation=plus
|GMAF=0.2291
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 40.7 | 51.3
| HCB | 5.9 | 45.9 | 48.1
| JPT | 8.0 | 50.4 | 41.6
| YRI | 6.2 | 26.7 | 67.1
| ASW | 0.0 | 28.1 | 71.9
| CHB | 5.9 | 45.9 | 48.1
| CHD | 6.5 | 49.1 | 44.4
| GIH | 6.9 | 37.6 | 55.4
| LWK | 1.8 | 29.1 | 69.1
| MEX | 0.0 | 19.0 | 81.0
| MKK | 1.9 | 32.1 | 66.0
| TSI | 9.8 | 33.3 | 56.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23453885
  |Trait=Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
  |Title=Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
  |RiskAllele=T
  |Pval=7E-6
  |OR=1.07
  |ORtxt=[1.04-1.12]
  |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}}