rs12636454
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12636454(C;C) |
Make rs12636454(C;T) |
Make rs12636454(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 12318715 |
Gene | PPARG |
is a | snp |
is | mentioned by |
dbSNP | rs12636454 |
dbSNP (classic) | rs12636454 |
ClinGen | rs12636454 |
ebi | rs12636454 |
HLI | rs12636454 |
Exac | rs12636454 |
Gnomad | rs12636454 |
Varsome | rs12636454 |
LitVar | rs12636454 |
Map | rs12636454 |
PheGenI | rs12636454 |
Biobank | rs12636454 |
1000 genomes | rs12636454 |
hgdp | rs12636454 |
ensembl | rs12636454 |
geneview | rs12636454 |
scholar | rs12636454 |
rs12636454 | |
pharmgkb | rs12636454 |
gwascentral | rs12636454 |
openSNP | rs12636454 |
23andMe | rs12636454 |
SNPshot | rs12636454 |
SNPdbe | rs12636454 |
MSV3d | rs12636454 |
GWAS Ctlg | rs12636454 |
GMAF | 0.2856 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23386649] Common Genetic Variants in Peroxisome Proliferator-Activated Receptor-γ (PPARG) and Type 2 Diabetes Risk Among Women's Health Initiative Postmenopausal Women
[PMID 20550665] Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population.