rs4764039
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4764039(C;C) |
Make rs4764039(C;T) |
Make rs4764039(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 13911527 |
Gene | GRIN2B |
is a | snp |
is | mentioned by |
dbSNP | rs4764039 |
dbSNP (classic) | rs4764039 |
ClinGen | rs4764039 |
ebi | rs4764039 |
HLI | rs4764039 |
Exac | rs4764039 |
Gnomad | rs4764039 |
Varsome | rs4764039 |
LitVar | rs4764039 |
Map | rs4764039 |
PheGenI | rs4764039 |
Biobank | rs4764039 |
1000 genomes | rs4764039 |
hgdp | rs4764039 |
ensembl | rs4764039 |
geneview | rs4764039 |
scholar | rs4764039 |
rs4764039 | |
pharmgkb | rs4764039 |
gwascentral | rs4764039 |
openSNP | rs4764039 |
23andMe | rs4764039 |
SNPshot | rs4764039 |
SNPdbe | rs4764039 |
MSV3d | rs4764039 |
GWAS Ctlg | rs4764039 |
GMAF | 0.1997 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21116278] |
Trait | |
Title | Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | 0.0049 [NR] unit increase (main effect) |