rs199498
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs199498(C;C) |
| Make rs199498(C;T) |
| Make rs199498(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 17 |
| Position | 46788237 |
| Gene | WNT3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs199498 |
| dbSNP (classic) | rs199498 |
| ClinGen | rs199498 |
| ebi | rs199498 |
| HLI | rs199498 |
| Exac | rs199498 |
| Gnomad | rs199498 |
| Varsome | rs199498 |
| LitVar | rs199498 |
| Map | rs199498 |
| PheGenI | rs199498 |
| Biobank | rs199498 |
| 1000 genomes | rs199498 |
| hgdp | rs199498 |
| ensembl | rs199498 |
| geneview | rs199498 |
| scholar | rs199498 |
| rs199498 | |
| pharmgkb | rs199498 |
| gwascentral | rs199498 |
| openSNP | rs199498 |
| 23andMe | rs199498 |
| SNPshot | rs199498 |
| SNPdbe | rs199498 |
| MSV3d | rs199498 |
| GWAS Ctlg | rs199498 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24511991 ]
|
| Trait | Parkinson's disease |
| Title | Identification of a novel Parkinson's disease locus via stratified genome-wide association study. |
| Risk Allele | T |
| P-val | 2E-6 |
| Odds Ratio | 1.35 [1.25-1.45] |
