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rs1805477

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1805477(C;T)
Make rs1805477(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position13561795
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs1805477
ebirs1805477
HLIrs1805477
Exacrs1805477
Varsomers1805477
Maprs1805477
PheGenIrs1805477
hapmaprs1805477
1000 genomesrs1805477
hgdprs1805477
ensemblrs1805477
gopubmedrs1805477
geneviewrs1805477
scholarrs1805477
googlers1805477
pharmgkbrs1805477
gwascentralrs1805477
openSNPrs1805477
23andMers1805477
23andMe allrs1805477
SNP Nexus

SNPshotrs1805477
SNPdbers1805477
MSV3drs1805477
GWAS Ctlgrs1805477
GMAF0.07943
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 22433450OA-icon.png] Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder