rs11159647
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11159647(A;A) |
| Make rs11159647(A;G) |
| Make rs11159647(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 84308865 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11159647 |
| dbSNP (classic) | rs11159647 |
| ClinGen | rs11159647 |
| ebi | rs11159647 |
| HLI | rs11159647 |
| Exac | rs11159647 |
| Gnomad | rs11159647 |
| Varsome | rs11159647 |
| LitVar | rs11159647 |
| Map | rs11159647 |
| PheGenI | rs11159647 |
| Biobank | rs11159647 |
| 1000 genomes | rs11159647 |
| hgdp | rs11159647 |
| ensembl | rs11159647 |
| geneview | rs11159647 |
| scholar | rs11159647 |
| rs11159647 | |
| pharmgkb | rs11159647 |
| gwascentral | rs11159647 |
| openSNP | rs11159647 |
| 23andMe | rs11159647 |
| SNPshot | rs11159647 |
| SNPdbe | rs11159647 |
| MSV3d | rs11159647 |
| GWAS Ctlg | rs11159647 |
| GMAF | 0.2759 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
genomeweb rs4420638 rs11159647 and rs3826656 were also significantly associated with Alzheimer's disease
The 'A' allele has been linked to to a somewhat higher risk of Alzheimer's disease, and a younger age at onset of the disease. [PMID 18976728
]
| GWAS snp | |
|---|---|
| PMID | [PMID 18976728]
|
| Trait | Alzheimer's disease |
| Title | Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | NR NR |
[PMID 19640594] Recent insights into the molecular genetics of dementia.
[PMID 20061627] Genome-wide scan of copy number variation in late-onset Alzheimer's disease.
[PMID 20574532] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.
