rs3755863
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3755863(A;A) |
| Make rs3755863(A;G) |
| Make rs3755863(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 23813899 |
| Gene | PPARGC1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3755863 |
| dbSNP (classic) | rs3755863 |
| ClinGen | rs3755863 |
| ebi | rs3755863 |
| HLI | rs3755863 |
| Exac | rs3755863 |
| Gnomad | rs3755863 |
| Varsome | rs3755863 |
| LitVar | rs3755863 |
| Map | rs3755863 |
| PheGenI | rs3755863 |
| Biobank | rs3755863 |
| 1000 genomes | rs3755863 |
| hgdp | rs3755863 |
| ensembl | rs3755863 |
| geneview | rs3755863 |
| scholar | rs3755863 |
| rs3755863 | |
| pharmgkb | rs3755863 |
| gwascentral | rs3755863 |
| openSNP | rs3755863 |
| 23andMe | rs3755863 |
| SNPshot | rs3755863 |
| SNPdbe | rs3755863 |
| MSV3d | rs3755863 |
| GWAS Ctlg | rs3755863 |
| GMAF | 0.371 |
| 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 20125101] Glucose levels and genetic variants across transcriptional pathways: interaction effects with BMI
[PMID 18588668
] Association between PPARGC1A polymorphisms and the occurrence of nonalcoholic fatty liver disease (NAFLD).
[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.
