rs145848414
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs145848414(A;A) |
Make rs145848414(A;G) |
Make rs145848414(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 174587111 |
is a | snp |
is | mentioned by |
dbSNP | rs145848414 |
dbSNP (classic) | rs145848414 |
ClinGen | rs145848414 |
ebi | rs145848414 |
HLI | rs145848414 |
Exac | rs145848414 |
Gnomad | rs145848414 |
Varsome | rs145848414 |
LitVar | rs145848414 |
Map | rs145848414 |
PheGenI | rs145848414 |
Biobank | rs145848414 |
1000 genomes | rs145848414 |
hgdp | rs145848414 |
ensembl | rs145848414 |
geneview | rs145848414 |
scholar | rs145848414 |
rs145848414 | |
pharmgkb | rs145848414 |
gwascentral | rs145848414 |
openSNP | rs145848414 |
23andMe | rs145848414 |
SNPshot | rs145848414 |
SNPdbe | rs145848414 |
MSV3d | rs145848414 |
GWAS Ctlg | rs145848414 |
GMAF | 0.01102 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23571587] |
Trait | Alzheimer's disease (late onset) |
Title | Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. |
Risk Allele | A |
P-val | 7E-8 |
Odds Ratio | 2.29 [1.69-3.09] |