UCP2, uncoupling protein 2, 7351

N. diseases: 235; N. variants: 5
Disease: Metabolic Syndrome X ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs660339
rs660339
Entrez Id: 7351
Gene Symbol: UCP2
UCP2
CUI: C0524620
Disease:
Metabolic Syndrome X 		0.020 GeneticVariation BEFREE Lack of association between the uncoupling protein-2 Ala55Val gene polymorphism and phenotypic features of the Metabolic Syndrome. 12385772 2002
dbSNP: rs660339
rs660339
Entrez Id: 7351
Gene Symbol: UCP2
UCP2
CUI: C0524620
Disease:
Metabolic Syndrome X 		0.020 GeneticVariation BEFREE There were no significant differences in the allele or genotype frequencies of the Ala55Val polymorphism between 55 patients with MSDR and 46 healthy controls. 9724080 1998