rs161802
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs161802(G;G) |
| Make rs161802(G;T) |
| Make rs161802(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 7982766 |
| Gene | PARK7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs161802 |
| dbSNP (classic) | rs161802 |
| ClinGen | rs161802 |
| ebi | rs161802 |
| HLI | rs161802 |
| Exac | rs161802 |
| Gnomad | rs161802 |
| Varsome | rs161802 |
| LitVar | rs161802 |
| Map | rs161802 |
| PheGenI | rs161802 |
| Biobank | rs161802 |
| 1000 genomes | rs161802 |
| hgdp | rs161802 |
| ensembl | rs161802 |
| geneview | rs161802 |
| scholar | rs161802 |
| rs161802 | |
| pharmgkb | rs161802 |
| gwascentral | rs161802 |
| openSNP | rs161802 |
| 23andMe | rs161802 |
| SNPshot | rs161802 |
| SNPdbe | rs161802 |
| MSV3d | rs161802 |
| GWAS Ctlg | rs161802 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24262325 ]
|
| Trait | Ischemic stroke |
| Title | Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. |
| Risk Allele | T |
| P-val | 2E-7 |
| Odds Ratio | 1.11 [1.08-1.16] |
