rs895767
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs895767(A;A) |
Make rs895767(A;C) |
Make rs895767(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 223158578 |
is a | snp |
is | mentioned by |
dbSNP | rs895767 |
dbSNP (classic) | rs895767 |
ClinGen | rs895767 |
ebi | rs895767 |
HLI | rs895767 |
Exac | rs895767 |
Gnomad | rs895767 |
Varsome | rs895767 |
LitVar | rs895767 |
Map | rs895767 |
PheGenI | rs895767 |
Biobank | rs895767 |
1000 genomes | rs895767 |
hgdp | rs895767 |
ensembl | rs895767 |
geneview | rs895767 |
scholar | rs895767 |
rs895767 | |
pharmgkb | rs895767 |
gwascentral | rs895767 |
openSNP | rs895767 |
23andMe | rs895767 |
SNPshot | rs895767 |
SNPdbe | rs895767 |
MSV3d | rs895767 |
GWAS Ctlg | rs895767 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24468470] |
Trait | Cognitive decline (age-related) |
Title | Genetic susceptibility to accelerated cognitive decline in the US Health and Retirement Study. |
Risk Allele | |
P-val | 7E-6 |
Odds Ratio | .01 [0.00572-0.01457] unit decrease |