LEPR, leptin receptor, 3953

N. diseases: 416; N. variants: 57
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.070 GeneticVariation disease BEFREE Associations of leptin and leptin receptor genetic variants with coronary artery disease: a meta-analysis. 31113873 2019
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.070 GeneticVariation disease BEFREE The aim of the present study was to evaluate four single nucleotide polymorphisms (SNPs) of APLNR genes (rs11544374 and rs948847), LEPR (rs1137101) and leptin (rs7799039) gene in patients with CAD and hypertension. 29883719 2018
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.070 Biomarker disease BEFREE The gene polymorphisms of adiponectin-encoding gene (ADIPOQ), leptin receptor (LEPR), apolipoprotein C3 (APOC3), peroxisome proliferator-activated receptors (PPAR), sterol regulatory elementbinding proteins (SREBP), transmembrane 6 superfamily member 2 (TM6SF2), microsomal triglyceride transfer protein (MTTP), tumor necrosis factors-alpha (TNF-α) and manganese superoxide dismutase (MnSOD) have been reported to be related to NAFLD and CAD. 26965314 2016
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.070 GeneticVariation disease BEFREE The interactions of CX3CL1, LEPR and IL-6 genes might increase the risk of CAD. 26191329 2015
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.070 GeneticVariation disease BEFREE We aimed to investigate the possible associations of serum leptin, leptin gene and leptin receptor gene polymorphism with HFNEF in patients with CAD. 21584748 2012
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.070 GeneticVariation disease BEFREE The 223A>G polymorphism of the leptin receptor gene and lipid-lowering efficacy of simvastatin in Chinese patients with coronary heart disease. 18854995 2009
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.070 GeneticVariation disease BEFREE SNPs rs6700896 in LEPR (OR, 1.06; 95% CI, 1.02 to 1.09; per minor allele), rs4537545 in IL6R (OR, 0.94; 95% CI, 0.91 to 0.97), and rs4420638 in the APOE-CI-CII cluster (OR, 1.16; 95% CI, 1.12 to 1.21) were all associated with risk of coronary heart disease. 19567438 2009