Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909244
rs121909244
PPARG
T 0.700 GeneticVariation CLINVAR Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes. 25157153

2014
dbSNP: rs121909244
rs121909244
PPARG
T 0.700 GeneticVariation CLINVAR Peroxisome proliferator-activated receptor-γ protects against vascular aging. 22461176

2012
dbSNP: rs121909244
rs121909244
PPARG
T 0.700 GeneticVariation CLINVAR Hypertension and abnormal fat distribution but not insulin resistance in mice with P465L PPARgamma. 15254591

2004
dbSNP: rs121909244
rs121909244
PPARG
T 0.700 GeneticVariation CLINVAR Dominant negative mutations in human PPARgamma associated with severe insulin resistance, diabetes mellitus and hypertension. 10622252

2000
dbSNP: rs121909244
rs121909244
PPARG
T 0.700 CausalMutation CLINVAR