rs1801282, PPARG

N. diseases: 131
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Acne
CUI: C0702166
Disease: Acne
0.020 GeneticVariation BEFREE Our results demonstrated the association of PPARγ Pro allele with susceptibility to AV in patients ≥20years and the influence of PPARγ Pro12Ala and C161T polymorphisms on the lipid and lipoprotein profile. 29120856 2018
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
0.020 GeneticVariation BEFREE Genotyping for Pro12Ala and Trp64Arg polymorphism in postmenopausal women may have the clinical benefit of predicting hyperglycaemia, thereby contributing to the prevention of diabetes mellitus development in the future. 29464546 2018
Acne Vulgaris
CUI: C0001144
Disease: Acne Vulgaris
0.020 GeneticVariation BEFREE Our results demonstrated the association of PPARγ Pro allele with susceptibility to AV in patients ≥20years and the influence of PPARγ Pro12Ala and C161T polymorphisms on the lipid and lipoprotein profile. 29120856 2018
Connective Tissue Diseases
CUI: C0009782
Disease: Connective Tissue Diseases
0.010 GeneticVariation BEFREE The aim of the research genetic study was to investigate the association between variants (C1431T and Pro12Ala) of the peroxisome proliferator-activated receptor (<i>PPARgamma-2</i>) gene, Trp64Arg polymorphism of the beta-3-adrenergic receptor gene and lipid profile in Polish population including group of 103 patients with connective tissue disease (CTD) and 103 sex-and age-matched controls in context of statin use. 29606859 2018
Sepsis
CUI: C0243026
Disease: Sepsis
0.010 GeneticVariation BEFREE For rs1801282, genotypes CG/CG+GG had lower risk of sepsis than genotype CC (0.55 [0.33-0.92], P = .024 and 0.57 [0.35-0.95], P = .03, respectively); the G allele was associated with decreased sepsis risk compared with the C allele (0.62 [0.39-1.01], P = .055). 29055064 2018
Neoplasms
CUI: C0027651
Disease: Neoplasms
0.010 GeneticVariation BEFREE We investigated associations between TNF-α <sup>-308</sup>G > A (rs1800629); PPARγ Pro<sup>12</sup>Ala (rs1801282); and IRS-1 Gly<sup>972</sup>Arg (rs1801278) polymorphisms and anthropometric variables, circulating levels of previously measured biomarkers, and tumor characteristics in 553 women enrolled in the Health, Eating, Activity, and Lifestyle Study, a multiethnic, prospective cohort study of women diagnosed with stage I-IIIA breast cancer between 1995 and 1999 (median follow-up 14.7 years). 29256014 2018
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
0.010 GeneticVariation BEFREE In a subgroup analysis by chronic hepatitis B virus (HBV)-infection status, age, sex, alcohol use, and smoking status, a significant association between <i>PPARG</i> rs1801282 C>G polymorphism and a decreased risk of HCC in male, ≥53 years, never-smoking, never-drinking, and nonchronic HBV-infection-status subgroups was found. 30122956 2018
Septicemia
CUI: C0036690
Disease: Septicemia
0.010 GeneticVariation BEFREE For rs1801282, genotypes CG/CG+GG had lower risk of sepsis than genotype CC (0.55 [0.33-0.92], P = .024 and 0.57 [0.35-0.95], P = .03, respectively); the G allele was associated with decreased sepsis risk compared with the C allele (0.62 [0.39-1.01], P = .055). 29055064 2018
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
0.010 GeneticVariation BEFREE In a subgroup analysis by chronic hepatitis B virus (HBV)-infection status, age, sex, alcohol use, and smoking status, a significant association between <i>PPARG</i> rs1801282 C>G polymorphism and a decreased risk of HCC in male, ≥53 years, never-smoking, never-drinking, and nonchronic HBV-infection-status subgroups was found. 30122956 2018
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation GWASCAT Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. 28869590 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE We found a significant association of Pro12Ala polymorphism of PPARγ2 gene with T2DM, however the genotypes showed statistically significant association only with few clinical parameters including body mass index, total cholesterol, and low-density lipoprotein (P < 0.05). 27567620 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.900 GeneticVariation BEFREE These findings suggest no significant association of p.Pro12Ala polymorphism with retinopathy in tested type 2 diabetic retinopathy patients as compared to T2DM individuals take as controls. 27427939 2017
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
0.100 GeneticVariation BEFREE Several variants <i>PPARG2</i> rs1801282 (<i>C>G</i>); <i>PPARGC1A</i> rs8192678 (<i>C>T</i>); <i>TCF7L2</i> rs7903146 (<i>C>T</i>); <i>LDLR</i> rs2228671 (<i>C>T</i>); <i>MTHFR</i> rs1801133 (<i>C>T</i>); <i>APOA5</i> rs662799 (<i>T>C</i>); <i>GCKR</i> rs1260326 (<i>C>T</i>); <i>FTO</i> rs9939609 (<i>T>A</i>); <i>MC4R</i> rs17782313 (<i>T>C</i>) were genotyped in 168 pregnant Caucasian women with or without GDM by High Resolution Melting (HRM) analysis. 28133617 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
0.100 GeneticVariation BEFREE In conclusion, our study indicates that <i>PPARG</i> rs1801282 C>G polymorphism might decrease the risk of overall CRC. 29246001 2017
Obesity
CUI: C0028754
Disease: Obesity
0.100 GeneticVariation BEFREE To further elucidate the role of genetics in obesity onset, we performed a candidate-gene association study in a young and sportive Italian population by testing the association of functional polymorphisms in ACE (rs4646994), FTO (rs9939609), MC4R (rs17782313) and PPARG (rs1801282) genes with body mass index (BMI) and waist-to-height ratio (WHtR). 28090739 2017
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
0.060 GeneticVariation BEFREE Cognitive decline and the PPAR-γ Pro12Ala genotype: variation by sex and ethnicity. 28181642 2017
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
0.050 GeneticVariation BEFREE To our knowledge, this is the first report of association analysis of p.Pro12Ala polymorphism in PPARγ in DR patients from India. 27427939 2017
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
0.040 GeneticVariation BEFREE The stratified analysis revealed <i>PPARG</i> rs1801282 C>G polymorphism also had a tendency of decreased risk to colon cancer (CG <i>vs</i>. 29246001 2017
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
0.040 GeneticVariation BEFREE The stratified analysis revealed <i>PPARG</i> rs1801282 C>G polymorphism also had a tendency of decreased risk to colon cancer (CG <i>vs</i>. 29246001 2017
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
0.040 GeneticVariation BEFREE Cognitive decline and the PPAR-γ Pro12Ala genotype: variation by sex and ethnicity. 28181642 2017
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.020 GeneticVariation BEFREE The subgroup analysis stratified by ethnicity showed that the significant association between the PPARG Pro12Ala polymorphism and EH was only detected in the Asian subgroup. 28727849 2017
Heart Failure, Diastolic
CUI: C1135196
Disease: Heart Failure, Diastolic
0.010 GeneticVariation BEFREE The study aimed to assess the clinical significance of selected single nucleotide polymorphisms (SNPs) in patients with diastolic heart failure (HF): inflammation [-174 G/C Interleukin -6 (IL-6) rs1800795, tumor necrosis factor (TNF)-608 G/A rs1800629], fibrosis [Arg25Pro transforming growth factor β (TGF β) rs1800471], endothelial function [-786 T/C nitric oxide synthase (NOS) rs2070744], glucose and lipid metabolism [Pro12Ala peroxisome proliferator activated receptor (PPAR)γ rs1801282], and vitamin D metabolism [cytochrome P450 27B1 (CYP27B1) C-1260A].110 patients with HF with preserved and mid-range ejection fraction (HFpEF and HFmrEF) were recruited. 28827564 2017
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
0.010 GeneticVariation BEFREE These findings suggest no significant association of p.Pro12Ala polymorphism with retinopathy in tested type 2 diabetic retinopathy patients as compared to T2DM individuals take as controls. 27427939 2017
Squamous cell carcinoma of esophagus
0.010 GeneticVariation BEFREE In conclusion, our findings highlight that <i>PPARG</i> rs1801282 C>G and rs3856806 C>T polymorphisms are candidates for susceptibility to ESCC in the eastern Chinese Han population. 29200867 2017