rs147845115
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs147845115(A;A) |
Make rs147845115(A;G) |
Make rs147845115(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 51484976 |
Gene | SLC4A8 |
is a | snp |
is | mentioned by |
dbSNP | rs147845115 |
dbSNP (classic) | rs147845115 |
ClinGen | rs147845115 |
ebi | rs147845115 |
HLI | rs147845115 |
Exac | rs147845115 |
Gnomad | rs147845115 |
Varsome | rs147845115 |
LitVar | rs147845115 |
Map | rs147845115 |
PheGenI | rs147845115 |
Biobank | rs147845115 |
1000 genomes | rs147845115 |
hgdp | rs147845115 |
ensembl | rs147845115 |
geneview | rs147845115 |
scholar | rs147845115 |
rs147845115 | |
pharmgkb | rs147845115 |
gwascentral | rs147845115 |
openSNP | rs147845115 |
23andMe | rs147845115 |
SNPshot | rs147845115 |
SNPdbe | rs147845115 |
MSV3d | rs147845115 |
GWAS Ctlg | rs147845115 |
GMAF | 0.01148 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23535033] |
Trait | Alzheimer's disease (cognitive decline) |
Title | Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. |
Risk Allele | |
P-val | 3E-7 |
Odds Ratio | .29 unit decrease |