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rs1806201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1806201(A;A)
Make rs1806201(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position13564574
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs1806201
ebirs1806201
HLIrs1806201
Exacrs1806201
Varsomers1806201
Maprs1806201
PheGenIrs1806201
hapmaprs1806201
1000 genomesrs1806201
hgdprs1806201
ensemblrs1806201
gopubmedrs1806201
geneviewrs1806201
scholarrs1806201
googlers1806201
pharmgkbrs1806201
gwascentralrs1806201
openSNPrs1806201
23andMers1806201
23andMe allrs1806201
SNP Nexus

SNPshotrs1806201
SNPdbers1806201
MSV3drs1806201
GWAS Ctlgrs1806201
GMAF0.3072
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 16911840] Association study of polymorphisms in N-methyl-D-aspartate receptor 2B subunits (GRIN2B) gene with Korean alcoholism

[PMID 15812607] Polymorphisms in the NMDA subunit 2B are not associated with alcohol dependence and alcohol withdrawal-induced seizures and delirium tremens.

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

[PMID 20882066] Association between NMDA receptor subunit 2b gene polymorphism and Alzheimer's disease in Chinese Han population in Shanghai.

[PMID 21749895] Variations in the GRIN2B gene are associated with risky decision-making.

[PMID 21827795] Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization.


ClinVar
Risk rs1806201(A;A)
Alt rs1806201(A;A)
Reference rs1806201(G;G)
Significance Probable-non-pathogenic
Disease not provided not specified
Variation info
Gene GRIN2B
CLNDBN not provided not specified
Reversed 0
HGVS NC_000012.11:g.13717508G>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000084728.1, RCV000117194.2,



[PMID 24114429] A study of N-methyl-D-aspartate receptor gene (GRIN2B) variants as predictors of treatment-resistant major depression


[PMID 22484476] N-methyl-D-aspartate receptor 2B subunit (GRIN2B) gene variation is associated with alerting, but not with orienting and conflicting in the Attention Network Test.


[PMID 22850629] Glutamatergic GRIN2B and polyaminergic ODC1 genes in suicide attempts: associations and gene-environment interactions with childhood/adolescent physical assault.


[PMID 23408766OA-icon.png] Assessment of NMDA receptor genes (GRIN2A, GRIN2B and GRIN2C) as candidate genes in the development of degenerative lumbar scoliosis.


[PMID 23644918OA-icon.png] Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset.


[PMID 25660313] Meta-analysis of six genes (BDNF, DRD1, DRD3, DRD4, GRIN2B and MAOA) involved in neuroplasticity and the risk for alcohol dependence


[PMID 27325396] Dopamine D3 receptor Ser9Gly variant is associated with impulse control disorders in Parkinson's disease patients.