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rs4998386

From SNPedia

Orientationplus
Stabilizedplus
Make rs4998386(C;C)
Make rs4998386(C;T)
Make rs4998386(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position9976688
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs4998386
dbSNP (classic)rs4998386
ClinGenrs4998386
ebirs4998386
HLIrs4998386
Exacrs4998386
Gnomadrs4998386
Varsomers4998386
LitVarrs4998386
Maprs4998386
PheGenIrs4998386
Biobankrs4998386
1000 genomesrs4998386
hgdprs4998386
ensemblrs4998386
geneviewrs4998386
scholarrs4998386
googlers4998386
pharmgkbrs4998386
gwascentralrs4998386
openSNPrs4998386
23andMers4998386
SNPshotrs4998386
SNPdbers4998386
MSV3drs4998386
GWAS Ctlgrs4998386
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 24915238OA-icon.png] Caffeine Interaction with Glutamate Receptor Gene GRIN2A: Parkinson's Disease in Swedish Population


[PMID 31942532OA-icon.png] Glutamate ionotropic receptor NMDA type subunit 2A (GRIN2A) gene polymorphism (rs4998386) and Parkinson's disease susceptibility: A meta-analysis.