rs466433
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs466433(A;A) |
| Make rs466433(A;G) |
| Make rs466433(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 21 |
| Position | 26171645 |
| Gene | APP, LOC107985473 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs466433 |
| dbSNP (classic) | rs466433 |
| ClinGen | rs466433 |
| ebi | rs466433 |
| HLI | rs466433 |
| Exac | rs466433 |
| Gnomad | rs466433 |
| Varsome | rs466433 |
| LitVar | rs466433 |
| Map | rs466433 |
| PheGenI | rs466433 |
| Biobank | rs466433 |
| 1000 genomes | rs466433 |
| hgdp | rs466433 |
| ensembl | rs466433 |
| geneview | rs466433 |
| scholar | rs466433 |
| rs466433 | |
| pharmgkb | rs466433 |
| gwascentral | rs466433 |
| openSNP | rs466433 |
| 23andMe | rs466433 |
| SNPshot | rs466433 |
| SNPdbe | rs466433 |
| MSV3d | rs466433 |
| GWAS Ctlg | rs466433 |
| Max Magnitude | 0 |
[PMID 25631235] Genetic Association Between APP, ADAM10 Gene Polymorphism, and Sporadic Alzheimer's Disease in the Chinese Population
