rs11770757
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs11770757(A;A) |
| Make rs11770757(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 134063193 |
| Gene | EXOC4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11770757 |
| dbSNP (classic) | rs11770757 |
| ClinGen | rs11770757 |
| ebi | rs11770757 |
| HLI | rs11770757 |
| Exac | rs11770757 |
| Gnomad | rs11770757 |
| Varsome | rs11770757 |
| LitVar | rs11770757 |
| Map | rs11770757 |
| PheGenI | rs11770757 |
| Biobank | rs11770757 |
| 1000 genomes | rs11770757 |
| hgdp | rs11770757 |
| ensembl | rs11770757 |
| geneview | rs11770757 |
| scholar | rs11770757 |
| rs11770757 | |
| pharmgkb | rs11770757 |
| gwascentral | rs11770757 |
| openSNP | rs11770757 |
| 23andMe | rs11770757 |
| SNPshot | rs11770757 |
| SNPdbe | rs11770757 |
| MSV3d | rs11770757 |
| GWAS Ctlg | rs11770757 |
| GMAF | 0.01928 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23535033 ]
|
| Trait | Alzheimer's disease (cognitive decline) |
| Title | Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. |
| Risk Allele | |
| P-val | 5E-7 |
| Odds Ratio | .16 unit decrease |
[PMID 18498660] Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study.
