rs2069442
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | normal | |
| (C;G) | normal | |
| (G;G) | 1.9x increased risk of Alzheimer's |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 151058118 |
| Gene | CDK5, SLC4A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2069442 |
| dbSNP (classic) | rs2069442 |
| ClinGen | rs2069442 |
| ebi | rs2069442 |
| HLI | rs2069442 |
| Exac | rs2069442 |
| Gnomad | rs2069442 |
| Varsome | rs2069442 |
| LitVar | rs2069442 |
| Map | rs2069442 |
| PheGenI | rs2069442 |
| Biobank | rs2069442 |
| 1000 genomes | rs2069442 |
| hgdp | rs2069442 |
| ensembl | rs2069442 |
| geneview | rs2069442 |
| scholar | rs2069442 |
| rs2069442 | |
| pharmgkb | rs2069442 |
| gwascentral | rs2069442 |
| openSNP | rs2069442 |
| 23andMe | rs2069442 |
| SNPshot | rs2069442 |
| SNPdbe | rs2069442 |
| MSV3d | rs2069442 |
| GWAS Ctlg | rs2069442 |
| GMAF | 0.3489 |
| Max Magnitude | 0 |
[PMID 18350355] (G;G) showed a 1.9-fold increased risk of Alzheimer's disease (95 % CI 1.16-3.10, p = 0.003)
[PMID 19615060
] No association of CDK5 genetic variants with Alzheimer's disease risk
[PMID 15717931] Identification of functional SNPs in the 5-prime flanking sequences of human genes.
