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rs4880213

From SNPedia

Orientationplus
Stabilizedplus
Make rs4880213(C;C)
Make rs4880213(C;T)
Make rs4880213(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position137136549
is asnp
is mentioned by
dbSNPrs4880213
ebirs4880213
HLIrs4880213
Exacrs4880213
Varsomers4880213
Maprs4880213
PheGenIrs4880213
hapmaprs4880213
1000 genomesrs4880213
hgdprs4880213
ensemblrs4880213
gopubmedrs4880213
geneviewrs4880213
scholarrs4880213
googlers4880213
pharmgkbrs4880213
gwascentralrs4880213
openSNPrs4880213
23andMers4880213
23andMe allrs4880213
SNP Nexus

SNPshotrs4880213
SNPdbers4880213
MSV3drs4880213
GWAS Ctlgrs4880213
GMAF0.4715
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20438806] Association analysis of GRIN1 and GRIN2B polymorphisms and Parkinson's disease in a hospital-based case-control study


[PMID 17728671] Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample.


[PMID 23840674OA-icon.png] Opposite roles of NMDA receptors in relapsing and primary progressive multiple sclerosis