rs4920608
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4920608(C;C) |
| Make rs4920608(C;T) |
| Make rs4920608(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 16992792 |
| Gene | ATP13A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4920608 |
| dbSNP (classic) | rs4920608 |
| ClinGen | rs4920608 |
| ebi | rs4920608 |
| HLI | rs4920608 |
| Exac | rs4920608 |
| Gnomad | rs4920608 |
| Varsome | rs4920608 |
| LitVar | rs4920608 |
| Map | rs4920608 |
| PheGenI | rs4920608 |
| Biobank | rs4920608 |
| 1000 genomes | rs4920608 |
| hgdp | rs4920608 |
| ensembl | rs4920608 |
| geneview | rs4920608 |
| scholar | rs4920608 |
| rs4920608 | |
| pharmgkb | rs4920608 |
| gwascentral | rs4920608 |
| openSNP | rs4920608 |
| 23andMe | rs4920608 |
| SNPshot | rs4920608 |
| SNPdbe | rs4920608 |
| MSV3d | rs4920608 |
| GWAS Ctlg | rs4920608 |
| GMAF | 0.4573 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22285144
] ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese
