Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs369841551
rs369841551
MC4R
A 0.700 CausalMutation CLINVAR Prevalence and phenotypic characterization of MC4R variants in a large pediatric cohort. 27654141

2017
dbSNP: rs369841551
rs369841551
MC4R
A 0.700 CausalMutation CLINVAR Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene. 12646665

2003
dbSNP: rs369841551
rs369841551
MC4R
A 0.700 CausalMutation CLINVAR The Protein Data Bank. 10592235

2000
dbSNP: rs369841551
rs369841551
MC4R
A 0.700 CausalMutation CLINVAR Several mutations in the melanocortin-4 receptor gene including a nonsense and a frameshift mutation associated with dominantly inherited obesity in humans. 10199800

1999