rs7657071
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7657071(A;A) |
Make rs7657071(A;C) |
Make rs7657071(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 23894851 |
Gene | PPARGC1A |
is a | snp |
is | mentioned by |
dbSNP | rs7657071 |
dbSNP (classic) | rs7657071 |
ClinGen | rs7657071 |
ebi | rs7657071 |
HLI | rs7657071 |
Exac | rs7657071 |
Gnomad | rs7657071 |
Varsome | rs7657071 |
LitVar | rs7657071 |
Map | rs7657071 |
PheGenI | rs7657071 |
Biobank | rs7657071 |
1000 genomes | rs7657071 |
hgdp | rs7657071 |
ensembl | rs7657071 |
geneview | rs7657071 |
scholar | rs7657071 |
rs7657071 | |
pharmgkb | rs7657071 |
gwascentral | rs7657071 |
openSNP | rs7657071 |
23andMe | rs7657071 |
SNPshot | rs7657071 |
SNPdbe | rs7657071 |
MSV3d | rs7657071 |
GWAS Ctlg | rs7657071 |
GMAF | 0.2502 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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