rs1800206, PPARA

N. diseases: 35
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO
0.700 SusceptibilityMutation CLINVAR
Diabetes Mellitus, Non-Insulin-Dependent
0.070 GeneticVariation BEFREE We suggest that the PPARA L162V polymorphism may have diverse effects on serum lipids and CHD risk depends on the presence of T2DM. 23583468 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.070 GeneticVariation BEFREE According to our study, the L162V SNP does not have a strong impact on the pathogenesis of type 2 diabetes or obesity. 18726867 2009
Diabetes Mellitus, Non-Insulin-Dependent
0.070 GeneticVariation BEFREE In conclusion, in a relative large-scale study of middle-aged whites we found no evidence of association between the PPARalpha Leu162Val polymorphism and obesity or type 2 diabetes. 17129741 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.070 GeneticVariation BEFREE We examined association between three PPARalpha gene polymorphisms (an A-->C variant in intron 1, the L162V variant, and the intron 7 G-->C variant) and age at diagnosis of type 2 diabetes in 912 Caucasian type 2 diabetic subjects. 15677519 2005
Diabetes Mellitus, Non-Insulin-Dependent
0.070 GeneticVariation BEFREE Association between the PPARalpha L162V polymorphism, plasma lipoprotein levels, and atherosclerotic disease in patients with diabetes mellitus type 2 and in nondiabetic controls. 15199365 2004
Diabetes Mellitus, Non-Insulin-Dependent
0.070 GeneticVariation BEFREE A polymorphism, L162V, in the peroxisome proliferator-activated receptor alpha (PPARalpha) gene is associated with lower body mass index in patients with non-insulin-dependent diabetes mellitus. 11409711 2001
Diabetes Mellitus, Non-Insulin-Dependent
0.070 GeneticVariation BEFREE We subsequently screened a sample of 121 patients newly diagnosed with type 2 diabetes and their age and sex-matched nondiabetic controls, recruited from the Saguenay-Lac-St-Jean region of Northeastern Quebec, for the presence of the L162V mutation by a PCR-RFLP based method. 10828087 2000
Obesity
CUI: C0028754
Disease: Obesity
0.060 GeneticVariation BEFREE GMDR analysis indicated a significant two-locus model (p=0.0107) involving rs1800206 and abdominal obesity, indicating a potential interaction among rs1800206 and abdominal obesity. 26671228 2016
Obesity
CUI: C0028754
Disease: Obesity
0.060 GeneticVariation BEFREE This study aimed to investigate the association of peroxisome proliferator-activated receptor (PPAR) genes PPARα L162V, PPARγ2 C161T and PPARδ T294C single nucleotide polymorphisms (SNPs) with obesity and metabolic syndrome (Met-S) in a multi-ethnic population in Kampar, Malaysia. 26673968 2015
Obesity
CUI: C0028754
Disease: Obesity
0.060 GeneticVariation BEFREE According to our study, the L162V SNP does not have a strong impact on the pathogenesis of type 2 diabetes or obesity. 18726867 2009
Obesity
CUI: C0028754
Disease: Obesity
0.060 GeneticVariation BEFREE In conclusion, in a relative large-scale study of middle-aged whites we found no evidence of association between the PPARalpha Leu162Val polymorphism and obesity or type 2 diabetes. 17129741 2007
Obesity
CUI: C0028754
Disease: Obesity
0.060 GeneticVariation BEFREE L162V was not associated with obesity, type 2 diabetes mellitus, hypercholesterolemia, or hypertriglyceridemia. 16297361 2005
Obesity
CUI: C0028754
Disease: Obesity
0.060 GeneticVariation BEFREE This study examined the effect a polymorphism (L162V) in the gene for peroxisome proliferator activated receptor (PPAR) alpha in the development of non-insulin-dependent diabetes mellitus (type 2 DM), obesity and hyperlipidaemia. 11409711 2001
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.040 GeneticVariation BEFREE We genotyped the Leu162Val polymorphism in 1383 patients with type 2 diabetes and 4401 control subjects with normal glucose tolerance (NGT) without showing any association between diabetes and genotype. 17129741 2007
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.040 GeneticVariation BEFREE In the placebo group, the G (162V) allele of rs1800206 increased the risk for diabetes by 1.9-fold (95% CI 1.05-3.58) and was associated with elevated levels of plasma glucose and insulin. 17317762 2007
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.040 GeneticVariation BEFREE The effect of the L162V polymorphism at the PPARA locus on CV risk depends on the presence of DM/IR. 16221474 2006
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.040 GeneticVariation BEFREE Overall, the PPARalpha haplotype signficantly influenced age at diagnosis (P = 0.027), with the C-L-C and C-V-C haplotypes (intron 1-L162V-intron 7) accelerating onset of diabetes by 5.9 (P = 0.02) and 10 (P = 0.03) years, respectively, as compared with the common A-L-G haplotype, and was associated with an odds ratio for early-onset diabetes (age at diagnosis </=45 years) of 3.75 (95% CI 1.65-8.56, P = 0.002). 15677519 2005
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.030 GeneticVariation BEFREE The results suggested that PPAR-alpha intron 7G/C and L162V, PPAR-delta +294T/C and PPAR-gamma C161T polymorphisms could affect CHD susceptibility, and C161T polymorphism might have different effects on CHD and ACS. 27512842 2016
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.030 GeneticVariation BEFREE This study aimed to investigate the association of peroxisome proliferator-activated receptor (PPAR) genes PPARα L162V, PPARγ2 C161T and PPARδ T294C single nucleotide polymorphisms (SNPs) with obesity and metabolic syndrome (Met-S) in a multi-ethnic population in Kampar, Malaysia. 26673968 2015
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
0.030 GeneticVariation BEFREE When the most common haplotype L-G (established by r</span>s1800206, rs4253778) was treated as the reference group, the V-G haplotype was associated with dyslipidemia (P < 0.001), higher TC and TG levels (P < 0.01). 24460649 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.030 GeneticVariation BEFREE We suggest that the PPARA L162V polymorphism may have diverse effects on serum lipids and CHD risk depends on the presence of T2DM. 23583468 2013
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.030 GeneticVariation BEFREE The frequency distribution of rare alleles for PPARα (L162V) and PPARγ (P12A and H449H) was compared using the chi square test in 363 HIV-1-infected patients classified according to the presence or absence of the metabolic syndrome after 48 months of follow-up on their first PI-containing regimen. 21877956 2012
Diabetes
CUI: C0011847
Disease: Diabetes
0.030 GeneticVariation BEFREE We genotyped the Leu162Val polymorphism in 1383 patients with type 2 diabetes and 4401 control subjects with normal glucose tolerance (NGT) without showing any association between diabetes and genotype. 17129741 2007
Diabetes
CUI: C0011847
Disease: Diabetes
0.030 GeneticVariation BEFREE In the placebo group, the G (162V) allele of rs1800206 increased the risk for diabetes by 1.9-fold (95% CI 1.05-3.58) and was associated with elevated levels of plasma glucose and insulin. 17317762 2007