rs13117172
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs13117172(C;T) |
| Make rs13117172(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 23878892 |
| Gene | PPARGC1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13117172 |
| dbSNP (classic) | rs13117172 |
| ClinGen | rs13117172 |
| ebi | rs13117172 |
| HLI | rs13117172 |
| Exac | rs13117172 |
| Gnomad | rs13117172 |
| Varsome | rs13117172 |
| LitVar | rs13117172 |
| Map | rs13117172 |
| PheGenI | rs13117172 |
| Biobank | rs13117172 |
| 1000 genomes | rs13117172 |
| hgdp | rs13117172 |
| ensembl | rs13117172 |
| geneview | rs13117172 |
| scholar | rs13117172 |
| rs13117172 | |
| pharmgkb | rs13117172 |
| gwascentral | rs13117172 |
| openSNP | rs13117172 |
| 23andMe | rs13117172 |
| SNPshot | rs13117172 |
| SNPdbe | rs13117172 |
| MSV3d | rs13117172 |
| GWAS Ctlg | rs13117172 |
| GMAF | 0.3356 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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
