MC4R, melanocortin 4 receptor, 4160

N. diseases: 149; N. variants: 58
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913564
rs121913564
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
CUI: C0028754
Disease:
Obesity
C 0.800 GeneticVariation CLINVAR Genetic variants in LEP, LEPR, and MC4R explain 30% of severe obesity in children from a consanguineous population. 26179253 2015
dbSNP: rs121913564
rs121913564
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
CUI: C0028754
Disease:
Obesity
C 0.800 GeneticVariation CLINVAR High prevalence of leptin and melanocortin-4 receptor gene mutations in children with severe obesity from Pakistani consanguineous families. 22463805 2012
dbSNP: rs121913564
rs121913564
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
CUI: C0028754
Disease:
Obesity
C 0.800 GeneticVariation CLINVAR We have studied the intracellular localization of four obesity-linked MC4R variants, P78L, R165W, I316S, and I317T, in immortalized neurons. 20631012 2010
dbSNP: rs121913564
rs121913564
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
CUI: C0028754
Disease:
Obesity
C 0.800 GeneticVariation CLINVAR Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms. 12588803 2003
dbSNP: rs121913564
rs121913564
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
CUI: C0028754
Disease:
Obesity
C 0.800 GeneticVariation CLINVAR Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene. 12646665 2003
dbSNP: rs121913564
rs121913564
Entrez Id: 4160
Gene Symbol: MC4R
MC4R
CUI: C0028754
Disease:
Obesity
0.800 GeneticVariation UNIPROT