Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1053049
rs1053049
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE A total of 156 subjects at an increased risk for type 2 diabetes were genotyped for rs1053049, rs6902123, and rs2267668 and participated in a LI program. 18252792 2008
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0028754
Disease:
Obesity
0.060 GeneticVariation BEFREE C-C haplotype, constructed from rs2016520 and rs9794 alleles, showed a significant protective effect for both abnormal weight and abdominal obesity. 26073637 2016
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0028754
Disease:
Obesity
0.060 GeneticVariation BEFREE rs2016520 and rs10865170 were associated with lower obesity risk. 23545576 2013
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0028754
Disease:
Obesity
0.060 GeneticVariation BEFREE Accumulated evidence suggests that the polymorphism rs2016520 in PPARD is associated with lipid metabolism, obesity, metabolic syndrome, and type 2 diabetes mellitus. 28128413 2017
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0028754
Disease:
Obesity
0.060 GeneticVariation BEFREE After adjustment for gender, age, and smoking status, it was found that the carriers of the C allele (TC + CC) of rs2016520 were associated with a decreased risk of abdominal obesity compared to the carriers of the TT genotype (mean difference = -2.63, 95% CI = -3.61--1.64, P < 0.0001). 23273766 2012
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0028754
Disease:
Obesity
0.060 GeneticVariation BEFREE Polymorphism of rs2016520 in gene PPARD has been associated with lipid metabolism, obesity, metabolic syndrome and type 2 diabetes mellitus (T2DM). 26915488 2016
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0028754
Disease:
Obesity
0.060 GeneticVariation BEFREE Previous studies have identified a single-nucleotide polymorphism in the gene encoding peroxisome proliferator-activated receptor-delta (PPARD), rs2016520, that is associated with changes in metabolic disease in some but not all studies, which suggests that PPARD agonists may have therapeutic benefits for the treatment of metabolic disorders, including dyslipidemia, type 2 diabetes, and obesity. 20200337 2010
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE Previous studies have identified a single-nucleotide polymorphism in the gene encoding peroxisome proliferator-activated receptor-delta (PPARD), rs2016520, that is associated with changes in metabolic disease in some but not all studies, which suggests that PPARD agonists may have therapeutic benefits for the treatment of metabolic disorders, including dyslipidemia, type 2 diabetes, and obesity. 20200337 2010
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE There was an association between rs2016520 and height in both patients with type 2 diabetes and controls without diabetes (combined P = 5 x 10(-5)). 19383774 2009
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE Polymorphism of rs2016520 in gene PPARD has been associated with lipid metabolism, obesity, metabolic syndrome and type 2 diabetes mellitus (T2DM). 26915488 2016
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.040 GeneticVariation BEFREE Accumulated evidence suggests that the polymorphism rs2016520 in PPARD is associated with lipid metabolism, obesity, metabolic syndrome, and type 2 diabetes mellitus. 28128413 2017
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0011849
Disease:
Diabetes Mellitus
0.020 GeneticVariation BEFREE No significant difference was found in either allelic frequency (P = 0.298) or genotype distribution (P = 0.151) of PPARD rs2016520 between T2DM patients and healthy subjects. 25311380 2015
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0009402
Disease:
Colorectal Carcinoma
0.020 GeneticVariation BEFREE In this study, whether the intratumoral heterogeneity of polymorphism of PPARD-87 T>C (rs2016520) existed and its influence in CRC were investigated. 30868900 2019
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0009402
Disease:
Colorectal Carcinoma
0.020 GeneticVariation BEFREE In conclusion, for the first time, the association between the +294T/C (rs2016520) polymorphism and colorectal cancer has been studied in Mexican patients. 28128413 2017
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0011849
Disease:
Diabetes Mellitus
0.020 GeneticVariation BEFREE There was an association between rs2016520 and height in both patients with type 2 diabetes and controls without diabetes (combined P = 5 x 10(-5)). 19383774 2009
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0011847
Disease:
Diabetes
0.010 GeneticVariation BEFREE There was an association between rs2016520 and height in both patients with type 2 diabetes and controls without diabetes (combined P = 5 x 10(-5)). 19383774 2009
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0010068
Disease:
Coronary heart disease
0.010 GeneticVariation BEFREE We found that the PPARD rs2016520-GG genotype decreased CHD risk in a Han Chinese population. 26125839 2015
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0242339
Disease:
Dyslipidemias
0.010 GeneticVariation BEFREE Previous studies have identified a single-nucleotide polymorphism in the gene encoding peroxisome proliferator-activated receptor-delta (PPARD), rs2016520, that is associated with changes in metabolic disease in some but not all studies, which suggests that PPARD agonists may have therapeutic benefits for the treatment of metabolic disorders, including dyslipidemia, type 2 diabetes, and obesity. 20200337 2010
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE Positive association between PPARD rs2016520 polymorphism and coronary heart disease in a Han Chinese population. 26125839 2015
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0007222
Disease:
Cardiovascular Diseases
0.010 GeneticVariation BEFREE The minor allele of rs2016520 and rs9794 in PPAR-δ and interaction between rs2016520 and non-smoking were associated with decreased risk of CVD. 28287878 2017
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE We investigated three frequent polymorphisms located in exons 4 (rs2016520) and 9 (rs3734254 and rs9794) of the PPARdelta gene (PPARD) for their putative influence on the risk of AD and on plasma levels of cholesterol, 24S-hydroxycholesterol and 27-hydroxycholesterol. 16979821 2006
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0006118
Disease:
Brain Neoplasms
0.010 GeneticVariation BEFREE We aimed to check the contribution of PPARD rs2016520 and lipid concentration to the risk of intracerebral hemorrhages (ICH) and brain tumors (BT) in Han Chinese. 25776471 2015
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0025517
Disease:
Metabolic Diseases
0.010 GeneticVariation BEFREE The objective of the study was to determine whether rs2016520 or other single-nucleotide polymorphism in the PPARD locus influenced the risk of developing various characteristics of metabolic disease. 20200337 2010
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE Positive association between PPARD rs2016520 polymorphism and coronary heart disease in a Han Chinese population. 26125839 2015
dbSNP: rs2016520
rs2016520
Entrez Id: 5467
Gene Symbol: PPARD
PPARD
CUI: C0006111
Disease:
Brain Diseases
0.010 GeneticVariation BEFREE PPARD rs2016520 polymorphism and circulating lipid levels connect with brain diseases in Han Chinese and suggest sex-dependent effects. 25776471 2015