rs732528
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs732528(A;A) |
Make rs732528(A;G) |
Make rs732528(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 50851864 |
is a | snp |
is | mentioned by |
dbSNP | rs732528 |
dbSNP (classic) | rs732528 |
ClinGen | rs732528 |
ebi | rs732528 |
HLI | rs732528 |
Exac | rs732528 |
Gnomad | rs732528 |
Varsome | rs732528 |
LitVar | rs732528 |
Map | rs732528 |
PheGenI | rs732528 |
Biobank | rs732528 |
1000 genomes | rs732528 |
hgdp | rs732528 |
ensembl | rs732528 |
geneview | rs732528 |
scholar | rs732528 |
rs732528 | |
pharmgkb | rs732528 |
gwascentral | rs732528 |
openSNP | rs732528 |
23andMe | rs732528 |
SNPshot | rs732528 |
SNPdbe | rs732528 |
MSV3d | rs732528 |
GWAS Ctlg | rs732528 |
GMAF | 0.1837 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 0.000007 |
Odds Ratio | 0.1106 [NR] unit decrease (main effect) |