rs10018239
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10018239(A;A) |
Make rs10018239(A;G) |
Make rs10018239(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 23853268 |
Gene | PPARGC1A |
is a | snp |
is | mentioned by |
dbSNP | rs10018239 |
dbSNP (classic) | rs10018239 |
ClinGen | rs10018239 |
ebi | rs10018239 |
HLI | rs10018239 |
Exac | rs10018239 |
Gnomad | rs10018239 |
Varsome | rs10018239 |
LitVar | rs10018239 |
Map | rs10018239 |
PheGenI | rs10018239 |
Biobank | rs10018239 |
1000 genomes | rs10018239 |
hgdp | rs10018239 |
ensembl | rs10018239 |
geneview | rs10018239 |
scholar | rs10018239 |
rs10018239 | |
pharmgkb | rs10018239 |
gwascentral | rs10018239 |
openSNP | rs10018239 |
23andMe | rs10018239 |
SNPshot | rs10018239 |
SNPdbe | rs10018239 |
MSV3d | rs10018239 |
GWAS Ctlg | rs10018239 |
GMAF | 0.3393 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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