rs1569476
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1569476(A;A) |
Make rs1569476(A;G) |
Make rs1569476(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 169639679 |
is a | snp |
is | mentioned by |
dbSNP | rs1569476 |
dbSNP (classic) | rs1569476 |
ClinGen | rs1569476 |
ebi | rs1569476 |
HLI | rs1569476 |
Exac | rs1569476 |
Gnomad | rs1569476 |
Varsome | rs1569476 |
LitVar | rs1569476 |
Map | rs1569476 |
PheGenI | rs1569476 |
Biobank | rs1569476 |
1000 genomes | rs1569476 |
hgdp | rs1569476 |
ensembl | rs1569476 |
geneview | rs1569476 |
scholar | rs1569476 |
rs1569476 | |
pharmgkb | rs1569476 |
gwascentral | rs1569476 |
openSNP | rs1569476 |
23andMe | rs1569476 |
SNPshot | rs1569476 |
SNPdbe | rs1569476 |
MSV3d | rs1569476 |
GWAS Ctlg | rs1569476 |
GMAF | 0.2888 |
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 | 3E-7 |
Odds Ratio | 0.0032 [NR] unit increase (main effect) |