Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE In particular, FTO and FABP2 gene polymorphisms were significantly associated with susceptibility to MS and obesity in this cohort. 28738793 2017
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE The FABP2 Ala54Thr polymorphism was significantly associated with obesity (AT vs AA: OR = 2.633, 95%CI = 1.065-6.663, P = 0.036; TT vs AA: OR = 4.160, 95%CI = 1.609-10.757, P = 0.003) and metabolic syndrome (TT vs AA: OR = 2.273, 95%CI = 1.242-4.156, P = 0.008) by logistic regression with adjustment for covariates. 25730055 2015
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE Correlations between FABP2 rs11724758 polymorphisms and components of MetS reveal that high-density lipoprotein cholesterol (HDL-c) levels are significantly higher in FABP2 rs11724758 AA genotype carrier compared with noncarriers, whereas triglycerides (TG) and fasting plasma glucose (FG) were to be significantly lower in the AA genotype carrier. 23911300 2013
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE The aim of this study was to investigate the association between FABP2 Ala54Thr genetic polymorphism and metabolic syndrome and some biochemical and anthropological parameters in elderly subjects. 22838187 2012
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE The aim of our study was to investigate the relationship between MS and Thr54 polymorphism in the FABP2 gene in obese patients. 20723947 2011
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE Thr54 allele carriers of the Ala54Thr variant of FABP2 gene have associations with metabolic syndrome and hypertriglyceridemia in urban South Indians. 16919542 2006
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE AGT T174M, GNB3 825C>T, and APOC3 -455T>C genotypes were significantly associated with MetS (P = 0.018, 0.0056, and 0.029, respectively) for female adults, whereas FABP2 A54T genotype was associated with MetS (P = 0.040) for female adolescents. 15869758 2006
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE The T54 variant of the FABP2 gene has shown an association with the insulin resistance syndrome in some, but not all, studies. 16718632 2006
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 Biomarker disease BEFREE The alanine (A) to threonine (T) substitution at codon 54 of the intestinal fatty acid-binding protein 2 (FABP2) has been associated with dyslipidaemia and other characteristics of the metabolic syndrome, which in turn is a risk factor for cerebrovascular disease. 16013194 2005
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 Biomarker disease BEFREE Controls carrying FABP2 Thr54 were more likely to have MS than noncarriers (Fisher's exact test P = 0.031; odds ratio = 6.9 with a 95% confidence interval of 1.1, 43.9). 15598690 2005
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE Our study suggests that the effects of FABP2 allelic variations on lipid traits are context dependent, indicating that this variant may play an important role in cardiovascular pathogenesis in the presence of IRS or hypertriglyceridemia. 15547295 2005
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE The Ala54Thr polymorphism of the FABP2 gene is not associated with CHD, markers of the metabolic syndrome, or the fatty acid profile of serum lipids in Finnish CHD patients. 12189904 2002
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 GeneticVariation disease BEFREE These results suggest that the FABP2 Thr54 allele may have a minor contribution to the insulin resistance syndrome in a white general population. 11423496 2001
Entrez Id: 2169
Gene Symbol: FABP2
FABP2
0.100 Biomarker disease BEFREE These findings suggest that FABP2 does not represent a major gene for Type 2 DM in this migrant Indian population living in Guadeloupe, but seems to be related to the metabolic insulin resistance syndrome. 10443326 1999