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rs1019385

From SNPedia

Orientationminus
Stabilizedplus
Make rs1019385(G;G)
Make rs1019385(G;T)
Make rs1019385(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position13981909
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs1019385
ebirs1019385
HLIrs1019385
Exacrs1019385
Varsomers1019385
Maprs1019385
PheGenIrs1019385
hapmaprs1019385
1000 genomesrs1019385
hgdprs1019385
ensemblrs1019385
gopubmedrs1019385
geneviewrs1019385
scholarrs1019385
googlers1019385
pharmgkbrs1019385
gwascentralrs1019385
openSNPrs1019385
23andMers1019385
23andMe allrs1019385
SNP Nexus

SNPshotrs1019385
SNPdbers1019385
MSV3drs1019385
GWAS Ctlgrs1019385
GMAF0.4293
Max Magnitude
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 19324536OA-icon.png] 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 16266783] Analysis of correlation between serum D-serine levels and functional promoter polymorphisms of GRIN2A and GRIN2B genes.


[PMID 18303265] Association analysis of GRIN2B, encoding N-methyl-D-aspartate receptor 2B subunit, and Alzheimer's disease.


[PMID 18983893] Association between NR2B subunit gene (GRIN2B) promoter polymorphisms and sporadic Alzheimer's disease in the North Chinese population.


[PMID 19911060OA-icon.png] Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint.