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rs12636454

From SNPedia

Orientationplus
Stabilizedplus
Make rs12636454(C;C)
Make rs12636454(C;T)
Make rs12636454(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position12318715
GenePPARG
is asnp
is mentioned by
dbSNPrs12636454
ebirs12636454
HLIrs12636454
Exacrs12636454
Varsomers12636454
Maprs12636454
PheGenIrs12636454
hapmaprs12636454
1000 genomesrs12636454
hgdprs12636454
ensemblrs12636454
gopubmedrs12636454
geneviewrs12636454
scholarrs12636454
googlers12636454
pharmgkbrs12636454
gwascentralrs12636454
openSNPrs12636454
23andMers12636454
23andMe allrs12636454
SNP Nexus

SNPshotrs12636454
SNPdbers12636454
MSV3drs12636454
GWAS Ctlgrs12636454
GMAF0.2856
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23386649OA-icon.png] Common Genetic Variants in Peroxisome Proliferator-Activated Receptor-γ (PPARG) and Type 2 Diabetes Risk Among Women's Health Initiative Postmenopausal Women


[PMID 20550665OA-icon.png] Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population.