rs4998386
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4998386(C;C) |
Make rs4998386(C;T) |
Make rs4998386(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 9976688 |
Gene | GRIN2A |
is a | snp |
is | mentioned by |
dbSNP | rs4998386 |
dbSNP (classic) | rs4998386 |
ClinGen | rs4998386 |
ebi | rs4998386 |
HLI | rs4998386 |
Exac | rs4998386 |
Gnomad | rs4998386 |
Varsome | rs4998386 |
LitVar | rs4998386 |
Map | rs4998386 |
PheGenI | rs4998386 |
Biobank | rs4998386 |
1000 genomes | rs4998386 |
hgdp | rs4998386 |
ensembl | rs4998386 |
geneview | rs4998386 |
scholar | rs4998386 |
rs4998386 | |
pharmgkb | rs4998386 |
gwascentral | rs4998386 |
openSNP | rs4998386 |
23andMe | rs4998386 |
SNPshot | rs4998386 |
SNPdbe | rs4998386 |
MSV3d | rs4998386 |
GWAS Ctlg | rs4998386 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24915238] Caffeine Interaction with Glutamate Receptor Gene GRIN2A: Parkinson's Disease in Swedish Population
[PMID 31942532] Glutamate ionotropic receptor NMDA type subunit 2A (GRIN2A) gene polymorphism (rs4998386) and Parkinson's disease susceptibility: A meta-analysis.