rs7791362
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7791362(C;C) |
Make rs7791362(C;T) |
Make rs7791362(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 8103297 |
is a | snp |
is | mentioned by |
dbSNP | rs7791362 |
dbSNP (classic) | rs7791362 |
ClinGen | rs7791362 |
ebi | rs7791362 |
HLI | rs7791362 |
Exac | rs7791362 |
Gnomad | rs7791362 |
Varsome | rs7791362 |
LitVar | rs7791362 |
Map | rs7791362 |
PheGenI | rs7791362 |
Biobank | rs7791362 |
1000 genomes | rs7791362 |
hgdp | rs7791362 |
ensembl | rs7791362 |
geneview | rs7791362 |
scholar | rs7791362 |
rs7791362 | |
pharmgkb | rs7791362 |
gwascentral | rs7791362 |
openSNP | rs7791362 |
23andMe | rs7791362 |
SNPshot | rs7791362 |
SNPdbe | rs7791362 |
MSV3d | rs7791362 |
GWAS Ctlg | rs7791362 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24684796] |
Trait | Cognitive function |
Title | Heritability and genetic association analysis of cognition in the Diabetes Heart Study. |
Risk Allele | C |
P-val | 4E-6 |
Odds Ratio | 2.78 [1.62-3.94] unit decrease |