rs10501570
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 1 | Normal risk of developing Parkinson's Disease |
| Make rs10501570(C;C) |
| Make rs10501570(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 84706803 |
| Gene | DLG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10501570 |
| dbSNP (classic) | rs10501570 |
| ClinGen | rs10501570 |
| ebi | rs10501570 |
| HLI | rs10501570 |
| Exac | rs10501570 |
| Gnomad | rs10501570 |
| Varsome | rs10501570 |
| LitVar | rs10501570 |
| Map | rs10501570 |
| PheGenI | rs10501570 |
| Biobank | rs10501570 |
| 1000 genomes | rs10501570 |
| hgdp | rs10501570 |
| ensembl | rs10501570 |
| geneview | rs10501570 |
| scholar | rs10501570 |
| rs10501570 | |
| pharmgkb | rs10501570 |
| gwascentral | rs10501570 |
| openSNP | rs10501570 |
| 23andMe | rs10501570 |
| SNPshot | rs10501570 |
| SNPdbe | rs10501570 |
| MSV3d | rs10501570 |
| GWAS Ctlg | rs10501570 |
| GMAF | 0.09734 |
| Max Magnitude | 1 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs10501570 |
| PubMedID | [PMID 17052657] |
| Condition | Parkinson's disease |
| Gene | DLG2 |
| Risk Allele | |
| pValue | 7.00E-006 |
| OR | 5 |
| 95% CI | 2.00-12.50 |
[PMID 19208180
] Detecting disease-associated genotype patterns.
[PMID 19429005
] Phactr2 and Parkinson's disease.
