rs4697046
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4697046(C;C) |
Make rs4697046(C;T) |
Make rs4697046(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 23834777 |
Gene | PPARGC1A |
is a | snp |
is | mentioned by |
dbSNP | rs4697046 |
dbSNP (classic) | rs4697046 |
ClinGen | rs4697046 |
ebi | rs4697046 |
HLI | rs4697046 |
Exac | rs4697046 |
Gnomad | rs4697046 |
Varsome | rs4697046 |
LitVar | rs4697046 |
Map | rs4697046 |
PheGenI | rs4697046 |
Biobank | rs4697046 |
1000 genomes | rs4697046 |
hgdp | rs4697046 |
ensembl | rs4697046 |
geneview | rs4697046 |
scholar | rs4697046 |
rs4697046 | |
pharmgkb | rs4697046 |
gwascentral | rs4697046 |
openSNP | rs4697046 |
23andMe | rs4697046 |
SNPshot | rs4697046 |
SNPdbe | rs4697046 |
MSV3d | rs4697046 |
GWAS Ctlg | rs4697046 |
GMAF | 0.377 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20426853] Association and interaction of PPAR-complex gene variants with latent traits of left ventricular diastolic function [PMID 18162502] PPARGC1A variation associated with DNA damage, diabetes, and cardiovascular diseases: the Boston Puerto Rican Health Study.