rs2076602
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2076602(A;A) |
| Make rs2076602(A;T) |
| Make rs2076602(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 16996703 |
| Gene | ATP13A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2076602 |
| dbSNP (classic) | rs2076602 |
| ClinGen | rs2076602 |
| ebi | rs2076602 |
| HLI | rs2076602 |
| Exac | rs2076602 |
| Gnomad | rs2076602 |
| Varsome | rs2076602 |
| LitVar | rs2076602 |
| Map | rs2076602 |
| PheGenI | rs2076602 |
| Biobank | rs2076602 |
| 1000 genomes | rs2076602 |
| hgdp | rs2076602 |
| ensembl | rs2076602 |
| geneview | rs2076602 |
| scholar | rs2076602 |
| rs2076602 | |
| pharmgkb | rs2076602 |
| gwascentral | rs2076602 |
| openSNP | rs2076602 |
| 23andMe | rs2076602 |
| SNPshot | rs2076602 |
| SNPdbe | rs2076602 |
| MSV3d | rs2076602 |
| GWAS Ctlg | rs2076602 |
| GMAF | 0.3085 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22285144
] ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese
