rs466448
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs466448(A;A) |
| Make rs466448(A;G) |
| Make rs466448(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 21 |
| Position | 26171790 |
| Gene | APP, LOC107985473 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs466448 |
| dbSNP (classic) | rs466448 |
| ClinGen | rs466448 |
| ebi | rs466448 |
| HLI | rs466448 |
| Exac | rs466448 |
| Gnomad | rs466448 |
| Varsome | rs466448 |
| LitVar | rs466448 |
| Map | rs466448 |
| PheGenI | rs466448 |
| Biobank | rs466448 |
| 1000 genomes | rs466448 |
| hgdp | rs466448 |
| ensembl | rs466448 |
| geneview | rs466448 |
| scholar | rs466448 |
| rs466448 | |
| pharmgkb | rs466448 |
| gwascentral | rs466448 |
| openSNP | rs466448 |
| 23andMe | rs466448 |
| SNPshot | rs466448 |
| SNPdbe | rs466448 |
| MSV3d | rs466448 |
| GWAS Ctlg | rs466448 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 25808939
] Cerebrospinal fluid Aβ42 levels and APP processing pathway genes in Parkinson's disease
