rs2970848
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2970848(A;A) |
| Make rs2970848(A;G) |
| Make rs2970848(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 23815404 |
| Gene | PPARGC1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2970848 |
| dbSNP (classic) | rs2970848 |
| ClinGen | rs2970848 |
| ebi | rs2970848 |
| HLI | rs2970848 |
| Exac | rs2970848 |
| Gnomad | rs2970848 |
| Varsome | rs2970848 |
| LitVar | rs2970848 |
| Map | rs2970848 |
| PheGenI | rs2970848 |
| Biobank | rs2970848 |
| 1000 genomes | rs2970848 |
| hgdp | rs2970848 |
| ensembl | rs2970848 |
| geneview | rs2970848 |
| scholar | rs2970848 |
| rs2970848 | |
| pharmgkb | rs2970848 |
| gwascentral | rs2970848 |
| openSNP | rs2970848 |
| 23andMe | rs2970848 |
| SNPshot | rs2970848 |
| SNPdbe | rs2970848 |
| MSV3d | rs2970848 |
| GWAS Ctlg | rs2970848 |
| GMAF | 0.3806 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21595954
] Association of PGC-1alpha polymorphisms with age of onset and risk of Parkinson's disease
[PMID 19200361] PGC-1alpha as modifier of onset age in Huntington disease.
[PMID 21211002] Localization of sequence variations in PGC-1alpha influence their modifying effect in Huntington disease.
[PMID 32174806] Hypermethylation of the Gene Coding for PGC-1α in Peripheral Blood Leukocytes of Patients With Parkinson's Disease.
