rs150519745
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs150519745(C;T) |
| Make rs150519745(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 1 |
| Position | 17000107 |
| Gene | ATP13A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs150519745 |
| dbSNP (classic) | rs150519745 |
| ClinGen | rs150519745 |
| ebi | rs150519745 |
| HLI | rs150519745 |
| Exac | rs150519745 |
| Gnomad | rs150519745 |
| Varsome | rs150519745 |
| LitVar | rs150519745 |
| Map | rs150519745 |
| PheGenI | rs150519745 |
| Biobank | rs150519745 |
| 1000 genomes | rs150519745 |
| hgdp | rs150519745 |
| ensembl | rs150519745 |
| geneview | rs150519745 |
| scholar | rs150519745 |
| rs150519745 | |
| pharmgkb | rs150519745 |
| gwascentral | rs150519745 |
| openSNP | rs150519745 |
| 23andMe | rs150519745 |
| SNPshot | rs150519745 |
| SNPdbe | rs150519745 |
| MSV3d | rs150519745 |
| GWAS Ctlg | rs150519745 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs150519745(T;T) |
| Alt | rs150519745(T;T) |
| Reference | Rs150519745(C;C) |
| Significance | Probable-Pathogenic |
| Disease | Parkinson disease 9 |
| Variation | info |
| Gene | ATP13A2 |
| CLNDBN | Parkinson disease 9 |
| Reversed | 0 |
| HGVS | NC_000001.10:g.17326602C>T |
| CLNSRC | Baylor College of Medicine |
| CLNACC | RCV000191065.1, |
