UCP2, uncoupling protein 2, 7351

N. diseases: 235; N. variants: 5
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: C0011849
Disease:
Diabetes Mellitus
0.050 GeneticVariation BEFREE Thus, UCP2 rs659366 A allele and rs660339 T allele are both related to longer LTL in subjects without diabetes, independent of cardiovascular risk factors. 27615599 2016
dbSNP: rs660339
rs660339
Entrez Id: 7351
Gene Symbol: UCP2
UCP2
CUI: C0011849
Disease:
Diabetes Mellitus
0.050 GeneticVariation BEFREE Recently, our group reported that the -866A/55Val/Ins haplotype (-866G/A, Ala55Val and Ins/Del polymorphisms) of the UCP2 gene was associated with increased risk for DR in patients with DM. 22134120 2012
dbSNP: rs660339
rs660339
Entrez Id: 7351
Gene Symbol: UCP2
UCP2
CUI: C0011849
Disease:
Diabetes Mellitus
0.050 GeneticVariation BEFREE The haplotype analyses further confirmed the association of Ala55Val with diabetes, where the haplotypes carrying the Ala allele were significantly higher in the cases compared to controls. 21175267 2011
dbSNP: rs660339
rs660339
Entrez Id: 7351
Gene Symbol: UCP2
UCP2
CUI: C0011849
Disease:
Diabetes Mellitus
0.050 GeneticVariation BEFREE Lack of association between uncoupling protein-2 Ala55Val polymorphism and incident diabetes in the atherosclerosis risk in communities study. 18496642 2008
dbSNP: rs660339
rs660339
Entrez Id: 7351
Gene Symbol: UCP2
UCP2
CUI: C0011849
Disease:
Diabetes Mellitus
0.050 GeneticVariation BEFREE We investigated the association of the commonly observed UCP2 Ala55Val (V) polymorphism with diabetes mellitus and impaired fasting glucose (IFG) among 3684 participants in the Coronary Artery Risk Development in Young Adults (CARDIA) study. 15951317 2005