{{Rsnum
|rsid=1019385
|Gene=GRIN2B
|Chromosome=12
|position=13981909
|Orientation=plus
|GMAF=0.4293
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=GRIN2B
}}[[rs1019385]] ( -200G/T ) is a SNP in close proximity to [[GRIN2B]] (Glutamate [NMDA] receptor subunit epsilon-2).

{{PMID|20421849}} significant effect of [[rs1019385]] genotype on habituation after acoustic stimulus noted

{{PMID|19324536|OA=1
}} small preliminary study (consisting of 16 psychotropic-naive pediatric patients) observed a significant association between [[rs1019385]] genotype and anterior cingulate cortex (ACC) glutamatergic concentration (but not occipital glutamatergic concentration)

{{PMID Auto
|PMID=16266783
|Title=Analysis of correlation between serum D-serine levels and functional promoter polymorphisms of GRIN2A and GRIN2B genes.
}}

{{PMID Auto
|PMID=18303265
|Title=Association analysis of GRIN2B, encoding N-methyl-D-aspartate receptor 2B subunit, and Alzheimer's disease.
}}

{{PMID Auto
|PMID=18983893
|Title=Association between NR2B subunit gene (GRIN2B) promoter polymorphisms and sporadic Alzheimer's disease in the North Chinese population.
}}

{{PMID Auto
|PMID=19911060
|Title=Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}