rs2970869
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2970869(A;A) |
| Make rs2970869(A;G) |
| Make rs2970869(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 23891746 |
| Gene | PPARGC1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2970869 |
| dbSNP (classic) | rs2970869 |
| ClinGen | rs2970869 |
| ebi | rs2970869 |
| HLI | rs2970869 |
| Exac | rs2970869 |
| Gnomad | rs2970869 |
| Varsome | rs2970869 |
| LitVar | rs2970869 |
| Map | rs2970869 |
| PheGenI | rs2970869 |
| Biobank | rs2970869 |
| 1000 genomes | rs2970869 |
| hgdp | rs2970869 |
| ensembl | rs2970869 |
| geneview | rs2970869 |
| scholar | rs2970869 |
| rs2970869 | |
| pharmgkb | rs2970869 |
| gwascentral | rs2970869 |
| openSNP | rs2970869 |
| 23andMe | rs2970869 |
| SNPshot | rs2970869 |
| SNPdbe | rs2970869 |
| MSV3d | rs2970869 |
| GWAS Ctlg | rs2970869 |
| GMAF | 0.2525 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19183932] PPARGC1A sequence variation and cardiovascular risk-factor levels: a study of the main genetic effects and gene x environment interactions in children from the European Youth Heart Study
[PMID 18162502
] PPARGC1A variation associated with DNA damage, diabetes, and cardiovascular diseases: the Boston Puerto Rican Health Study.
[PMID 19200361] PGC-1alpha as modifier of onset age in Huntington disease.
