rs1137101, LEPR

N. diseases: 77
Disease: Coronary Artery Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.020 GeneticVariation BEFREE However, no positive findings were observed for <i>LEPR</i> rs1137100 and rs1137101 variants in overall and subgroup analyses.<b>Conclusions:</b> Our meta-analysis suggested that <i>LEP</i> rs7799039 variant might affect individual susceptibility to CAD. 31113873 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.020 GeneticVariation 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