{{Rsnum
|rsid=1805502
|Gene=GRIN2B
|Chromosome=12
|position=13561247
|Orientation=plus
|GMAF=0.2498
|Gene_s=GRIN2B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 70.8 | 24.8 | 4.4
| HCB | 61.3 | 35.0 | 3.6
| JPT | 65.5 | 27.4 | 7.1
| YRI | 25.2 | 51.0 | 23.8
| ASW | 35.7 | 46.4 | 17.9
| CHB | 61.3 | 35.0 | 3.6
| CHD | 69.7 | 26.6 | 3.7
| GIH | 49.5 | 45.5 | 5.0
| LWK | 31.2 | 44.0 | 24.8
| MEX | 80.0 | 20.0 | 0.0
| MKK | 30.3 | 46.5 | 23.2
| TSI | 65.7 | 30.4 | 3.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=22433450
|Title=Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder
|OA=1
}}

{{PMID Auto
|PMID=22578441
|Title=Lack of an association between obsessive-compulsive disorder and polymorphisms in the 3' untranslated region of GRIN2B in a Chinese Han population
}}

{{PMID|16911840}} Association study of polymorphisms in N-methyl-D-aspartate receptor 2B subunits (GRIN2B) gene with Korean alcoholism.

{{PMID|19324536|OA=1
}} Glutamate receptor gene (GRIN2B) associated with reduced anterior cingulate glutamatergic concentration in pediatric obsessive-compulsive disorder.

{{PMID|20197096|OA=1
}} Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.

{{PMID|20537720}} Positive association between GRIN2B gene and bipolar disorder in the Chinese Han Population.

{{PMID Auto
|PMID=24114429
|Title=A study of N-methyl-D-aspartate receptor gene (GRIN2B) variants as predictors of treatment-resistant major depression
}}

{{PMID Auto
|PMID=23070074
|Title=Molecular evidence of N-methyl-D-aspartate receptor hypofunction in schizophrenia.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}