{{Rsnum
|rsid=8058295
|Gene=GRIN2A
|Chromosome=16
|position=9817529
|Orientation=plus
|GMAF=0.2567
|Gene_s=GRIN2A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 7.1 | 42.0 | 50.9
| HCB | 0.7 | 14.1 | 85.2
| JPT | 0.0 | 9.7 | 90.3
| YRI | 26.2 | 51.7 | 22.1
| ASW | 22.8 | 47.4 | 29.8
| CHB | 0.7 | 14.1 | 85.2
| CHD | 0.0 | 8.5 | 91.5
| GIH | 5.0 | 36.6 | 58.4
| LWK | 22.7 | 43.6 | 33.6
| MEX | 1.7 | 37.9 | 60.3
| MKK | 27.1 | 52.3 | 20.6
| TSI | 6.9 | 39.2 | 53.9
| 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=A
  |Pval=7E-6
  |OR=1.06
  |ORtxt=[1.04-1.09]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}