rs690705
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs690705(A;A) |
| Make rs690705(A;G) |
| Make rs690705(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 34080781 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs690705 |
| dbSNP (classic) | rs690705 |
| ClinGen | rs690705 |
| ebi | rs690705 |
| HLI | rs690705 |
| Exac | rs690705 |
| Gnomad | rs690705 |
| Varsome | rs690705 |
| LitVar | rs690705 |
| Map | rs690705 |
| PheGenI | rs690705 |
| Biobank | rs690705 |
| 1000 genomes | rs690705 |
| hgdp | rs690705 |
| ensembl | rs690705 |
| geneview | rs690705 |
| scholar | rs690705 |
| rs690705 | |
| pharmgkb | rs690705 |
| gwascentral | rs690705 |
| openSNP | rs690705 |
| 23andMe | rs690705 |
| SNPshot | rs690705 |
| SNPdbe | rs690705 |
| MSV3d | rs690705 |
| GWAS Ctlg | rs690705 |
| GMAF | 0.3251 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19749422] |
| Trait | Alzheimer's Disease |
| Title | Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease |
| Risk Allele | |
| P-val | 6E-7 |
| Odds Ratio | NR NR |
| GWAS snp | |
|---|---|
| PMID | [PMID 20061627 ]
|
| Trait | Alzheimer's disease |
| Title | Genome-wide scan of copy number variation in late-onset Alzheimer's disease. |
| Risk Allele | |
| P-val | 6E-7 |
| Odds Ratio | None None |
