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rs6902123

From SNPedia

Orientationplus
Stabilizedplus
Make rs6902123(C;C)
Make rs6902123(C;T)
Make rs6902123(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position35362644
GenePPARD
is asnp
is mentioned by
dbSNPrs6902123
ebirs6902123
HLIrs6902123
Exacrs6902123
Varsomers6902123
Maprs6902123
PheGenIrs6902123
hapmaprs6902123
1000 genomesrs6902123
hgdprs6902123
ensemblrs6902123
gopubmedrs6902123
geneviewrs6902123
scholarrs6902123
googlers6902123
pharmgkbrs6902123
gwascentralrs6902123
openSNPrs6902123
23andMers6902123
23andMe allrs6902123
SNP Nexus

SNPshotrs6902123
SNPdbers6902123
MSV3drs6902123
GWAS Ctlgrs6902123
GMAF0.213
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 18252792] rs1053049, rs6902123, and rs2267668 in PPARD affect Lifestyle Intervention induced changes in overall adiposity, hepatic fat storage, and relative muscle mass. Our findings provide a mechanistic explanation for the involvement of these genetic variations in the development of insulin resistance and type-2 diabetes.

[PMID 16804087] Single nucleotide polymorphisms of PPARD in combination with the Gly482Ser substitution of PGC-1A and the Pro12Ala substitution of PPARG2 predict the conversion from impaired glucose tolerance to type 2 diabetes: the STOP-NIDDM trial.

[PMID 18401448OA-icon.png] PPAR Genomics and Pharmacogenomics: Implications for Cardiovascular Disease.