LEPR, leptin receptor, 3953

N. diseases: 416; N. variants: 57
Disease: Somatotropin deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1137101
rs1137101
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0271561
Disease:
Somatotropin deficiency 		0.020 GeneticVariation BEFREE CONCLUSIONS Gene polymorphism of leptin (loci rs7799039) and leptin receptor (loci rs</span>1137101) are correlated with GHD susceptibility. 26915772 2016
dbSNP: rs1137101
rs1137101
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C0271561
Disease:
Somatotropin deficiency 		0.020 GeneticVariation BEFREE These results suggest LEPR Q223R SNP (rs1137101) is associated with outcomes of GH replacement therapy in ISS and GHD patients. 23009903 2012