rs10878226
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10878226(C;C) |
| Make rs10878226(C;G) |
| Make rs10878226(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 40223890 |
| Gene | LRRK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10878226 |
| dbSNP (classic) | rs10878226 |
| ClinGen | rs10878226 |
| ebi | rs10878226 |
| HLI | rs10878226 |
| Exac | rs10878226 |
| Gnomad | rs10878226 |
| Varsome | rs10878226 |
| LitVar | rs10878226 |
| Map | rs10878226 |
| PheGenI | rs10878226 |
| Biobank | rs10878226 |
| 1000 genomes | rs10878226 |
| hgdp | rs10878226 |
| ensembl | rs10878226 |
| geneview | rs10878226 |
| scholar | rs10878226 |
| rs10878226 | |
| pharmgkb | rs10878226 |
| gwascentral | rs10878226 |
| openSNP | rs10878226 |
| 23andMe | rs10878226 |
| SNPshot | rs10878226 |
| SNPdbe | rs10878226 |
| MSV3d | rs10878226 |
| GWAS Ctlg | rs10878226 |
| GMAF | 0.07208 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23115130
] Common variation in the LRRK2 gene is a risk factor for Parkinson's disease
