rs3764028
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs3764028(A;A) |
Make rs3764028(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 13982130 |
Gene | GRIN2B |
is a | snp |
is | mentioned by |
dbSNP | rs3764028 |
dbSNP (classic) | rs3764028 |
ClinGen | rs3764028 |
ebi | rs3764028 |
HLI | rs3764028 |
Exac | rs3764028 |
Gnomad | rs3764028 |
Varsome | rs3764028 |
LitVar | rs3764028 |
Map | rs3764028 |
PheGenI | rs3764028 |
Biobank | rs3764028 |
1000 genomes | rs3764028 |
hgdp | rs3764028 |
ensembl | rs3764028 |
geneview | rs3764028 |
scholar | rs3764028 |
rs3764028 | |
pharmgkb | rs3764028 |
gwascentral | rs3764028 |
openSNP | rs3764028 |
23andMe | rs3764028 |
SNPshot | rs3764028 |
SNPdbe | rs3764028 |
MSV3d | rs3764028 |
GWAS Ctlg | rs3764028 |
GMAF | 0.2107 |
Max Magnitude | 0 |
rs3764028 ( -421C/A ) is a SNP in close proximity to GRIN2B (Glutamate [NMDA] receptor subunit epsilon-2).
[PMID 18983893] significant differences in genotype between the North Chinese sporadic Alzheimer's patients (of which there were 362) and controls (of which there were 334). 34.69-39.79% decreased transcriptional activity (per luciferase reporter assay in SH-SY5Y and HeLa cell lines) noted for the C allele versus the A allele
[PMID 25693086] The relationship of TP53 and GRIN2B gene polymorphisms with risk of occurrence and progression of primary open-angle glaucoma in a Polish population