rs11525066
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common on affy axiom data |
Make rs11525066(A;A) |
Make rs11525066(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 78546660 |
Gene | MAGI2 |
is a | snp |
is | mentioned by |
dbSNP | rs11525066 |
dbSNP (classic) | rs11525066 |
ClinGen | rs11525066 |
ebi | rs11525066 |
HLI | rs11525066 |
Exac | rs11525066 |
Gnomad | rs11525066 |
Varsome | rs11525066 |
LitVar | rs11525066 |
Map | rs11525066 |
PheGenI | rs11525066 |
Biobank | rs11525066 |
1000 genomes | rs11525066 |
hgdp | rs11525066 |
ensembl | rs11525066 |
geneview | rs11525066 |
scholar | rs11525066 |
rs11525066 | |
pharmgkb | rs11525066 |
gwascentral | rs11525066 |
openSNP | rs11525066 |
23andMe | rs11525066 |
SNPshot | rs11525066 |
SNPdbe | rs11525066 |
MSV3d | rs11525066 |
GWAS Ctlg | rs11525066 |
GMAF | 0.04959 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19668339] |
Trait | Hippocampal atrophy |
Title | Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease |
Risk Allele | |
P-val | 0.000003 |
Odds Ratio | NR NR |