{{Rsnum
|rsid=1806194
|Gene=GRIN2B
|Chromosome=12
|position=13570193
|Orientation=plus
|GMAF=0.2328
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=GRIN2B
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 24.8 | 43.4 | 31.9
| HCB | 0.0 | 5.1 | 94.9
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.0 | 2.0 | 98.0
| ASW | 0.0 | 19.3 | 80.7
| CHB | 0.0 | 5.1 | 94.9
| CHD | 0.0 | 1.8 | 98.2
| GIH | 5.0 | 34.7 | 60.4
| LWK | 0.0 | 10.9 | 89.1
| MEX | 17.2 | 63.8 | 19.0
| MKK | 3.8 | 34.0 | 62.2
| TSI | 14.7 | 46.1 | 39.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=21919190
|Title=Association of GRIN1 and GRIN2A-D With schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}