rs10513788
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10513788(A;A) |
Make rs10513788(A;T) |
Make rs10513788(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 3 |
Position | 182403785 |
is a | snp |
is | mentioned by |
dbSNP | rs10513788 |
dbSNP (classic) | rs10513788 |
ClinGen | rs10513788 |
ebi | rs10513788 |
HLI | rs10513788 |
Exac | rs10513788 |
Gnomad | rs10513788 |
Varsome | rs10513788 |
LitVar | rs10513788 |
Map | rs10513788 |
PheGenI | rs10513788 |
Biobank | rs10513788 |
1000 genomes | rs10513788 |
hgdp | rs10513788 |
ensembl | rs10513788 |
geneview | rs10513788 |
scholar | rs10513788 |
rs10513788 | |
pharmgkb | rs10513788 |
gwascentral | rs10513788 |
openSNP | rs10513788 |
23andMe | rs10513788 |
SNPshot | rs10513788 |
SNPdbe | rs10513788 |
MSV3d | rs10513788 |
GWAS Ctlg | rs10513788 |
Max Magnitude | 0 |
? | (A;A) (A;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 | T |
P-val | 5E-6 |
Odds Ratio | 2.69 [1.56-3.82] unit decrease |