rs11158026
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11158026(C;C) |
| Make rs11158026(C;T) |
| Make rs11158026(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 14 |
| Position | 54882151 |
| Gene | GCH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11158026 |
| dbSNP (classic) | rs11158026 |
| ClinGen | rs11158026 |
| ebi | rs11158026 |
| HLI | rs11158026 |
| Exac | rs11158026 |
| Gnomad | rs11158026 |
| Varsome | rs11158026 |
| LitVar | rs11158026 |
| Map | rs11158026 |
| PheGenI | rs11158026 |
| Biobank | rs11158026 |
| 1000 genomes | rs11158026 |
| hgdp | rs11158026 |
| ensembl | rs11158026 |
| geneview | rs11158026 |
| scholar | rs11158026 |
| rs11158026 | |
| pharmgkb | rs11158026 |
| gwascentral | rs11158026 |
| openSNP | rs11158026 |
| 23andMe | rs11158026 |
| SNPshot | rs11158026 |
| SNPdbe | rs11158026 |
| MSV3d | rs11158026 |
| GWAS Ctlg | rs11158026 |
| Max Magnitude | 0 |
rs11158026(T) allele carriers show a slight increase in risk for Parkinson's disease, based on a study of ~200 patients; odds ratio 1.23, p = 0.048 (i.e. on the border of being considered statistically non-significant).[PMID 27871051
]
