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rs1797912

From SNPedia

Orientationplus
Stabilizedplus
Make rs1797912(A;A)
Make rs1797912(A;C)
Make rs1797912(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position12428740
GenePPARG
is asnp
is mentioned by
dbSNPrs1797912
ebirs1797912
HLIrs1797912
Exacrs1797912
Varsomers1797912
Maprs1797912
PheGenIrs1797912
hapmaprs1797912
1000 genomesrs1797912
hgdprs1797912
ensemblrs1797912
gopubmedrs1797912
geneviewrs1797912
scholarrs1797912
googlers1797912
pharmgkbrs1797912
gwascentralrs1797912
openSNPrs1797912
23andMers1797912
23andMe allrs1797912
SNP Nexus

SNPshotrs1797912
SNPdbers1797912
MSV3drs1797912
GWAS Ctlgrs1797912
GMAF0.3384
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 19543210] PPARG Genotype Accounts for Part of Individual Variation in Body Weight Reduction in Response to Calorie Restriction


[PMID 20426853OA-icon.png] Association and interaction of PPAR-complex gene variants with latent traits of left ventricular diastolic function.