rs1509269
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs1509269(C;T) |
| Make rs1509269(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 137832570 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1509269 |
| dbSNP (classic) | rs1509269 |
| ClinGen | rs1509269 |
| ebi | rs1509269 |
| HLI | rs1509269 |
| Exac | rs1509269 |
| Gnomad | rs1509269 |
| Varsome | rs1509269 |
| LitVar | rs1509269 |
| Map | rs1509269 |
| PheGenI | rs1509269 |
| Biobank | rs1509269 |
| 1000 genomes | rs1509269 |
| hgdp | rs1509269 |
| ensembl | rs1509269 |
| geneview | rs1509269 |
| scholar | rs1509269 |
| rs1509269 | |
| pharmgkb | rs1509269 |
| gwascentral | rs1509269 |
| openSNP | rs1509269 |
| 23andMe | rs1509269 |
| SNPshot | rs1509269 |
| SNPdbe | rs1509269 |
| MSV3d | rs1509269 |
| GWAS Ctlg | rs1509269 |
| GMAF | 0.09458 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
rs1509269 increases susceptibility to Parkinson's disease 1.71 times for carriers of the C allele [PMID 16252231
]
[PMID 16685661] Genomewide association, Parkinson disease, and PARK10.
[PMID 16685662] No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.
[PMID 16685663] A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.
