LEPR, leptin receptor, 3953

N. diseases: 416; N. variants: 57
Disease: Metabolic Syndrome X ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3790433
rs3790433
Entrez Id: 3953;54741
Gene Symbol: LEPR;LEPROT
LEPR;LEPROT
CUI: C0524620
Disease:
Metabolic Syndrome X 		0.010 GeneticVariation BEFREE Homozygosity for the LEPR rs3790433 G allele was associated with insulin resistance, which may predispose to increased MetS risk. 20032477 2010