rs6821591
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6821591(C;C) |
| Make rs6821591(C;T) |
| Make rs6821591(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 23795377 |
| Gene | PPARGC1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6821591 |
| dbSNP (classic) | rs6821591 |
| ClinGen | rs6821591 |
| ebi | rs6821591 |
| HLI | rs6821591 |
| Exac | rs6821591 |
| Gnomad | rs6821591 |
| Varsome | rs6821591 |
| LitVar | rs6821591 |
| Map | rs6821591 |
| PheGenI | rs6821591 |
| Biobank | rs6821591 |
| 1000 genomes | rs6821591 |
| hgdp | rs6821591 |
| ensembl | rs6821591 |
| geneview | rs6821591 |
| scholar | rs6821591 |
| rs6821591 | |
| pharmgkb | rs6821591 |
| gwascentral | rs6821591 |
| openSNP | rs6821591 |
| 23andMe | rs6821591 |
| SNPshot | rs6821591 |
| SNPdbe | rs6821591 |
| MSV3d | rs6821591 |
| GWAS Ctlg | rs6821591 |
| GMAF | 0.4229 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21595954
] Association of PGC-1alpha polymorphisms with age of onset and risk of Parkinson's disease
[PMID 19133136] The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease.
[PMID 21211002] Localization of sequence variations in PGC-1alpha influence their modifying effect in Huntington disease.
