rs682705
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs682705(C;C) |
| Make rs682705(C;T) |
| Make rs682705(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 54171744 |
| Gene | CYB5RL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs682705 |
| dbSNP (classic) | rs682705 |
| ClinGen | rs682705 |
| ebi | rs682705 |
| HLI | rs682705 |
| Exac | rs682705 |
| Gnomad | rs682705 |
| Varsome | rs682705 |
| LitVar | rs682705 |
| Map | rs682705 |
| PheGenI | rs682705 |
| Biobank | rs682705 |
| 1000 genomes | rs682705 |
| hgdp | rs682705 |
| ensembl | rs682705 |
| geneview | rs682705 |
| scholar | rs682705 |
| rs682705 | |
| pharmgkb | rs682705 |
| gwascentral | rs682705 |
| openSNP | rs682705 |
| 23andMe | rs682705 |
| SNPshot | rs682705 |
| SNPdbe | rs682705 |
| MSV3d | rs682705 |
| GWAS Ctlg | rs682705 |
| GMAF | 0.3375 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 16252231
] High-resolution whole-genome association study of Parkinson disease.
[PMID 16685661] Genomewide association, Parkinson disease, and PARK10.
[PMID 16685662] No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.
