rs7520966
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7520966(C;C) |
| Make rs7520966(C;T) |
| Make rs7520966(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 54179589 |
| Gene | CYB5RL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7520966 |
| dbSNP (classic) | rs7520966 |
| ClinGen | rs7520966 |
| ebi | rs7520966 |
| HLI | rs7520966 |
| Exac | rs7520966 |
| Gnomad | rs7520966 |
| Varsome | rs7520966 |
| LitVar | rs7520966 |
| Map | rs7520966 |
| PheGenI | rs7520966 |
| Biobank | rs7520966 |
| 1000 genomes | rs7520966 |
| hgdp | rs7520966 |
| ensembl | rs7520966 |
| geneview | rs7520966 |
| scholar | rs7520966 |
| rs7520966 | |
| pharmgkb | rs7520966 |
| gwascentral | rs7520966 |
| openSNP | rs7520966 |
| 23andMe | rs7520966 |
| SNPshot | rs7520966 |
| SNPdbe | rs7520966 |
| MSV3d | rs7520966 |
| GWAS Ctlg | rs7520966 |
| GMAF | 0.3343 |
| 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.
[PMID 16685663] A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.
[PMID 17052658] Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.
[PMID 17332845] Meta-analysis in genome-wide association datasets: strategies and application in Parkinson disease.
