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 |
