rs1805192, PPARG

N. diseases: 121
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
BODY MASS INDEX, MODIFIER OF
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
0.700 SusceptibilityMutation CLINVAR
OBESITY, MODIFIER OF
CUI: C1832250
Disease: OBESITY, MODIFIER OF
0.700 SusceptibilityMutation CLINVAR
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
0.700 SusceptibilityMutation CLINVAR
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
0.700 SusceptibilityMutation CLINVAR
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE (1) To determine the allele and genotype frequency of the Pro12Ala PPARgamma2 amino acid variant in a Polish population; (2) To search for the association of the Pro12Ala polymorphism with T2DM in the examined population. 14581147 2003
Obesity
CUI: C0028754
Disease: Obesity
0.100 GeneticVariation BEFREE Obesity and Pro12Ala Polymorphism of Peroxisome Proliferator-Activated Receptor-Gamma Gene in Healthy Adults: A Systematic Review and Meta-Analysis. 26361038 2015
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
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
Diabetes
CUI: C0011847
Disease: Diabetes
0.100 GeneticVariation BEFREE Diabetes genomics research has illuminated single nucleotide polymorphism (SNP) in several genes including, fat mass and obesity associated (FTO) (rs9939609 and rs9926289), potassium voltage-gated channel subfamily J member 11 (rs5219), SLC30A 8 (rs13266634) and peroxisome proliferator-activated receptor gamma 2 (rs1805192). 31823921 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.100 GeneticVariation BEFREE Diabetes genomics research has illuminated single nucleotide polymorphism (SNP) in several genes including, fat mass and obesity associated (FTO) (rs9939609 and rs9926289), potassium voltage-gated channel subfamily J member 11 (rs5219), SLC30A 8 (rs13266634) and peroxisome proliferator-activated receptor gamma 2 (rs1805192). 31823921 2019
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE Pro12Ala substitution in the peroxisome proliferator-activated receptor-gamma is associated with increased leptin levels in women with type-2 diabetes mellitus. 12218380 2002
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
0.050 GeneticVariation BEFREE Pro12Ala polymorphism in the peroxisome proliferator-activated receptor-gamma (PPAR-gamma) gene and risk of prostate cancer among men in a large cancer prevention study. 12609711 2003
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
0.050 GeneticVariation BEFREE Pro12Ala polymorphism in the peroxisome proliferator-activated receptor-gamma (PPAR-gamma) gene and risk of prostate cancer among men in a large cancer prevention study. 12609711 2003
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
0.020 GeneticVariation BEFREE P12A PPARgamma did not significantly interact with BMI, WHR, energy intake, and energy expenditure to alter risk of colon or rectal cancer. 15860437 2005
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE Pro12Ala polymorphism of the PPARG2 gene is associated with type 2 diabetes mellitus and peripheral insulin sensitivity in a population with a high intake of oleic acid. 16920849 2006
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.100 GeneticVariation BEFREE Pro12Ala polymorphism of the peroxisome proliferatoractivated receptor-gamma gene is associated with metabolic syndrome and surrogate measures of insulin resistance in healthy men: interaction with smoking status. 19745552 2009
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
0.070 GeneticVariation BEFREE Pro12Ala polymorphism in the PPARG gene contributes to the development of diabetic nephropathy in Chinese type 2 diabetic patients. 19837787 2010
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
0.090 GeneticVariation BEFREE Pro12Ala, a missense mutation in exon 2 of PPARG, reduces transcriptional activity of PPARgamma2 and is shown to be associated with increased insulin sensitivity and protection from T2D. 20368233 2010
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
0.100 GeneticVariation BEFREE Pro12Ala PPAR γ2 gene polymorphism in PCOS women: the role of compounds regulating satiety. 21827375 2012
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
0.100 GeneticVariation BEFREE Pro12Ala polymorphism was significantly associated with the susceptibility of PCOS (odds ratio [OR] 0.74, 95 % confidence interval [CI] [0.61, 0.90] for allele; OR 0.70, 95 % CI [0.57, 0.86] for genotype). 22527903 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.100 GeneticVariation BEFREE Pro12Ala mutation decreases PPARG activity and resistance to NIDDM. 22937051 2012
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
0.100 GeneticVariation BEFREE Pro12Ala polymorphism of PPARγ showed significant association with decreased PCOS susceptibility. 23748472 2013
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
0.050 GeneticVariation BEFREE Pro 12Ala and Ala203Pro polymorphisms did not modify the association between the iAs methylation capacity and BC. 27557380 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
0.050 GeneticVariation BEFREE Pro 12Ala and Ala203Pro polymorphisms did not modify the association between the iAs methylation capacity and BC. 27557380 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.100 GeneticVariation BEFREE Pro12Ala missense mutation of the peroxisome proliferator activated receptor gamma and diabetes mellitus. 9918859 1999