rs11155313
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11155313(A;A) |
| Make rs11155313(A;G) |
| Make rs11155313(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 143640440 |
| Gene | PHACTR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11155313 |
| dbSNP (classic) | rs11155313 |
| ClinGen | rs11155313 |
| ebi | rs11155313 |
| HLI | rs11155313 |
| Exac | rs11155313 |
| Gnomad | rs11155313 |
| Varsome | rs11155313 |
| LitVar | rs11155313 |
| Map | rs11155313 |
| PheGenI | rs11155313 |
| Biobank | rs11155313 |
| 1000 genomes | rs11155313 |
| hgdp | rs11155313 |
| ensembl | rs11155313 |
| geneview | rs11155313 |
| scholar | rs11155313 |
| rs11155313 | |
| pharmgkb | rs11155313 |
| gwascentral | rs11155313 |
| openSNP | rs11155313 |
| 23andMe | rs11155313 |
| SNPshot | rs11155313 |
| SNPdbe | rs11155313 |
| MSV3d | rs11155313 |
| GWAS Ctlg | rs11155313 |
| GMAF | 0.2525 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Four case-control series were combined along with previous GWAS results, yielding a 1.3x increased risk for Parkinson's disease among rs11155313 minor allele carriers.[PMID 19429005
]
[PMID 16252231] High-resolution whole-genome association study of Parkinson disease.
