LEP, leptin, 3952

N. diseases: 931; N. variants: 15
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894023
rs104894023
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease:
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.800 GeneticVariation UNIPROT Biologically inactive leptin and early-onset extreme obesity. 25551525 2015
dbSNP: rs104894023
rs104894023
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease:
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.800 GeneticVariation UNIPROT A leptin missense mutation associated with hypogonadism and morbid obesity. 9500540 1998
dbSNP: rs104894023
rs104894023
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease:
LEPTIN DEFICIENCY OR DYSFUNCTION 		T 0.800 CausalMutation CLINVAR
dbSNP: rs1554394014
rs1554394014
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease:
LEPTIN DEFICIENCY OR DYSFUNCTION 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs724159998
rs724159998
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease:
LEPTIN DEFICIENCY OR DYSFUNCTION 		0.700 GeneticVariation UNIPROT