rs11012
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common on affy axiom data |
| Make rs11012(A;A) |
| Make rs11012(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 45436075 |
| Gene | PLEKHM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11012 |
| dbSNP (classic) | rs11012 |
| ClinGen | rs11012 |
| ebi | rs11012 |
| HLI | rs11012 |
| Exac | rs11012 |
| Gnomad | rs11012 |
| Varsome | rs11012 |
| LitVar | rs11012 |
| Map | rs11012 |
| PheGenI | rs11012 |
| Biobank | rs11012 |
| 1000 genomes | rs11012 |
| hgdp | rs11012 |
| ensembl | rs11012 |
| geneview | rs11012 |
| scholar | rs11012 |
| rs11012 | |
| pharmgkb | rs11012 |
| gwascentral | rs11012 |
| openSNP | rs11012 |
| 23andMe | rs11012 |
| SNPshot | rs11012 |
| SNPdbe | rs11012 |
| MSV3d | rs11012 |
| GWAS Ctlg | rs11012 |
| GMAF | 0.1065 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20070850 ]
|
| Trait | Parkinson's disease |
| Title | Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease |
| Risk Allele | T |
| P-val | 6E-8 |
| Odds Ratio | 1.43 [1.27-1.61] |
[PMID 18985386] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
