LEPR, leptin receptor, 3953

N. diseases: 416; N. variants: 57
Disease: Androgen-Insensitivity Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2767485
rs2767485
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0039585
Disease:
Androgen-Insensitivity Syndrome 		0.010 GeneticVariation BEFREE Polymorphism of rs2767485 in LEPR gene is associated with the occurrence of AIS, suggesting LEPR is a predisposition gene. 26731704 2015