{{Rsnum
|rsid=1805476
|Gene=GRIN2B
|Chromosome=12
|position=13561429
|Orientation=plus
|GMAF=0.4348
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=GRIN2B
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 44.2 | 44.2 | 11.5
| HCB | 5.1 | 37.2 | 57.7
| JPT | 7.1 | 29.2 | 63.7
| YRI | 78.9 | 19.0 | 2.0
| ASW | 61.4 | 33.3 | 5.3
| CHB | 5.1 | 37.2 | 57.7
| CHD | 3.7 | 28.4 | 67.9
| GIH | 26.7 | 48.5 | 24.8
| LWK | 80.0 | 19.1 | 0.9
| MEX | 29.3 | 62.1 | 8.6
| MKK | 64.1 | 32.7 | 3.2
| TSI | 36.3 | 42.2 | 21.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=20438806
|Title=Association analysis of GRIN1 and GRIN2B polymorphisms and Parkinson's disease in a hospital-based case-control study
}}

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

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

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