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rs11146020

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs11146020(C;C)
Make rs11146020(C;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137138632
GeneGRIN1
is asnp
is mentioned by
dbSNPrs11146020
ebirs11146020
HLIrs11146020
Exacrs11146020
Varsomers11146020
Maprs11146020
PheGenIrs11146020
hapmaprs11146020
1000 genomesrs11146020
hgdprs11146020
ensemblrs11146020
gopubmedrs11146020
geneviewrs11146020
scholarrs11146020
googlers11146020
pharmgkbrs11146020
gwascentralrs11146020
openSNPrs11146020
23andMers11146020
23andMe allrs11146020
SNP Nexus

SNPshotrs11146020
SNPdbers11146020
MSV3drs11146020
GWAS Ctlgrs11146020
GMAF0.1189
Max Magnitude0
located in 5' UTR of GRIN1

[PMID 16476413] significant (p = .0000013) assoc. w/ schizophrenia in a sample of 2455 Han Chinese

[PMID 17728671] mentioned w/ possible schizophrenia association in a sample of 677 Germans (354 patients, 323 controls), but the initial association did not survive multiple correction

OMIM138249
DescGLUTAMATE RECEPTOR, IONOTROPIC, N-METHYL-D-ASPARTATE, SUBUNIT 1; GRIN1
Variant
Relatedalso


[PMID 18979923] [The association between glutamate receptor gene SNP and schizophrenia].


[PMID 21332319] Gene-gene interaction analyses between NMDA receptor subunit and dopamine receptor gene variants and clozapine response.


[PMID 23880023] Genetic variation of GRIN1 confers vulnerability to methamphetamine-dependent psychosis in a Thai population