rs9980664
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9980664(A;A) |
Make rs9980664(A;C) |
Make rs9980664(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 33362204 |
is a | snp |
is | mentioned by |
dbSNP | rs9980664 |
dbSNP (classic) | rs9980664 |
ClinGen | rs9980664 |
ebi | rs9980664 |
HLI | rs9980664 |
Exac | rs9980664 |
Gnomad | rs9980664 |
Varsome | rs9980664 |
LitVar | rs9980664 |
Map | rs9980664 |
PheGenI | rs9980664 |
Biobank | rs9980664 |
1000 genomes | rs9980664 |
hgdp | rs9980664 |
ensembl | rs9980664 |
geneview | rs9980664 |
scholar | rs9980664 |
rs9980664 | |
pharmgkb | rs9980664 |
gwascentral | rs9980664 |
openSNP | rs9980664 |
23andMe | rs9980664 |
SNPshot | rs9980664 |
SNPdbe | rs9980664 |
MSV3d | rs9980664 |
GWAS Ctlg | rs9980664 |
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 | 3E-6 |
Odds Ratio | .03 [0.01569-0.03866] unit increase |