rs1137100, LEPR

N. diseases: 39
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
0.010 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