rs7656250
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs7656250(C;C) |
| Make rs7656250(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 23864393 |
| Gene | PPARGC1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7656250 |
| dbSNP (classic) | rs7656250 |
| ClinGen | rs7656250 |
| ebi | rs7656250 |
| HLI | rs7656250 |
| Exac | rs7656250 |
| Gnomad | rs7656250 |
| Varsome | rs7656250 |
| LitVar | rs7656250 |
| Map | rs7656250 |
| PheGenI | rs7656250 |
| Biobank | rs7656250 |
| 1000 genomes | rs7656250 |
| hgdp | rs7656250 |
| ensembl | rs7656250 |
| geneview | rs7656250 |
| scholar | rs7656250 |
| rs7656250 | |
| pharmgkb | rs7656250 |
| gwascentral | rs7656250 |
| openSNP | rs7656250 |
| 23andMe | rs7656250 |
| SNPshot | rs7656250 |
| SNPdbe | rs7656250 |
| MSV3d | rs7656250 |
| GWAS Ctlg | rs7656250 |
| GMAF | 0.2654 |
| 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
[PMID 19828207] Evaluation of the association between the PPARGC1A genetic polymorphisms and type 2 diabetes in Han Chinese population
[PMID 25977930
] Genetic Associations of PPARGC1A with Type 2 Diabetes: Differences among Populations with African Origins
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 4
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
