rs11248051
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common on affy axiom data |
| Make rs11248051(C;T) |
| Make rs11248051(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 864544 |
| Gene | GAK |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11248051 |
| dbSNP (classic) | rs11248051 |
| ClinGen | rs11248051 |
| ebi | rs11248051 |
| HLI | rs11248051 |
| Exac | rs11248051 |
| Gnomad | rs11248051 |
| Varsome | rs11248051 |
| LitVar | rs11248051 |
| Map | rs11248051 |
| PheGenI | rs11248051 |
| Biobank | rs11248051 |
| 1000 genomes | rs11248051 |
| hgdp | rs11248051 |
| ensembl | rs11248051 |
| geneview | rs11248051 |
| scholar | rs11248051 |
| rs11248051 | |
| pharmgkb | rs11248051 |
| gwascentral | rs11248051 |
| openSNP | rs11248051 |
| 23andMe | rs11248051 |
| SNPshot | rs11248051 |
| SNPdbe | rs11248051 |
| MSV3d | rs11248051 |
| GWAS Ctlg | rs11248051 |
| GMAF | 0.08448 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20711177 ]
|
| Trait | |
| Title | Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease |
| Risk Allele | T |
| P-val | 3E-9 |
| Odds Ratio | 1.46 [1.29-1.65] |
[PMID 22451204] Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2
[PMID 18985386] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
[PMID 21281506] A unified framework for multi-locus association analysis of both common and rare variants.
