rs17329669
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 |
| Make rs17329669(A;G) |
| Make rs17329669(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 36812324 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17329669 |
| dbSNP (classic) | rs17329669 |
| ClinGen | rs17329669 |
| ebi | rs17329669 |
| HLI | rs17329669 |
| Exac | rs17329669 |
| Gnomad | rs17329669 |
| Varsome | rs17329669 |
| LitVar | rs17329669 |
| Map | rs17329669 |
| PheGenI | rs17329669 |
| Biobank | rs17329669 |
| 1000 genomes | rs17329669 |
| hgdp | rs17329669 |
| ensembl | rs17329669 |
| geneview | rs17329669 |
| scholar | rs17329669 |
| rs17329669 | |
| pharmgkb | rs17329669 |
| gwascentral | rs17329669 |
| openSNP | rs17329669 |
| 23andMe | rs17329669 |
| SNPshot | rs17329669 |
| SNPdbe | rs17329669 |
| MSV3d | rs17329669 |
| GWAS Ctlg | rs17329669 |
| GMAF | 0.07668 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
rs17329669 is an intergenic SNP on chromosome 7 between the AOAH gene and the ELMO1 gene (genes involved in neutrophils / possibly immune related).
rs17329669 (G) was associated with Parkinson's disease in a discordant sibling study [PMID 16252231
]
No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening. [PMID 16685662]
A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan. [PMID 16685663]
