Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1557670950
rs1557670950
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
CUI: C3554225
Disease:
LEPTIN RECEPTOR DEFICIENCY
C 0.700 CausalMutation CLINVAR