LEPR, leptin receptor, 3953

N. diseases: 416; N. variants: 57
Disease: Liver diseases ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1137100
rs1137100
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0023895
Disease:
Liver diseases 		0.010 GeneticVariation BEFREE This study suggests that rs1137100, specifically the G allele, is associated with a less severe form of liver disease in patients with NAFLD. 23278404 2013