rs3736265
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs3736265(A;A) |
| Make rs3736265(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 23813084 |
| Gene | PPARGC1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3736265 |
| dbSNP (classic) | rs3736265 |
| ClinGen | rs3736265 |
| ebi | rs3736265 |
| HLI | rs3736265 |
| Exac | rs3736265 |
| Gnomad | rs3736265 |
| Varsome | rs3736265 |
| LitVar | rs3736265 |
| Map | rs3736265 |
| PheGenI | rs3736265 |
| Biobank | rs3736265 |
| 1000 genomes | rs3736265 |
| hgdp | rs3736265 |
| ensembl | rs3736265 |
| geneview | rs3736265 |
| scholar | rs3736265 |
| rs3736265 | |
| pharmgkb | rs3736265 |
| gwascentral | rs3736265 |
| openSNP | rs3736265 |
| 23andMe | rs3736265 |
| SNPshot | rs3736265 |
| SNPdbe | rs3736265 |
| MSV3d | rs3736265 |
| GWAS Ctlg | rs3736265 |
| GMAF | 0.1088 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19828207] Evaluation of the association between the PPARGC1A genetic polymorphisms and type 2 diabetes in Han Chinese population
[PMID 16642433
] Polymorphism in maternal LRP8 gene is associated with fetal growth.
[PMID 17187763] Analysis of PGC-1alpha variants Gly482Ser and Thr612Met concerning their PPARgamma2-coactivation function.
[PMID 18162502] PPARGC1A variation associated with DNA damage, diabetes, and cardiovascular diseases: the Boston Puerto Rican Health Study.
[PMID 18588668] Association between PPARGC1A polymorphisms and the occurrence of nonalcoholic fatty liver disease (NAFLD).
[PMID 18599530] Ser1369Ala variant in sulfonylurea receptor gene ABCC8 is associated with antidiabetic efficacy of gliclazide in Chinese type 2 diabetic patients.
[PMID 19133136] The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease.
[PMID 20426853] Association and interaction of PPAR-complex gene variants with latent traits of left ventricular diastolic function.
[PMID 23741228] Lack of Genetic Associations of PPAR-γ and PGC-1α with Alzheimer's Disease and Parkinson's Disease with Dementia
[PMID 24383721] A single nucleotide polymorphism in the coding region of PGC-1alpha is a male-specific modifier of Huntington disease age-at-onset in a large European cohort
[PMID 32721231] Assessment of PPARGC1A, PPARGC1B, and PON1 Genetic Polymorphisms in Esophageal Squamous Cell Carcinoma Susceptibility in the Eastern Chinese Han Population: A Case-Control Study Involving 2351 Subjects.
