rs3135506, APOA5

N. diseases: 26
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.070 GeneticVariation BEFREE In this study, we aimed to determine the association of single nucleotide polymorphisms including: rs662799, rs3135506 and rs2075291 in the apolipoprotein A-V (APOA5) gene in relation to MetS component like triglyceride and HDL-C level in Tehran Lipid and Glucose Study (TLGS). 26702748 2016
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.070 GeneticVariation BEFREE Two common variants of ApoA5 (namely -1131T>C in the promoter region and c.56C>G in the coding region) with the risk of MetS were analyzed. 22905904 2012
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.070 GeneticVariation BEFREE The minor allele of rs9939609 (FTO), rs7903146 (TCF7L2), C56G (APOA5), T1131C (APOA5), C482T (APOC3), C455T (APOC3) and 174G>C (IL6) were more prevalent in subjects with MetS, whereas the minor allele of Taq-1B (CETP) was less prevalent in subjects with the MetS. 21749608 2011
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.070 GeneticVariation BEFREE Here we determined four haplotype-tagging polymorphisms (T-1131C, IVS3+G476A, T1259C, and C56G), and studied the distribution of the naturally occurring major haplotype profiles in MS. 19692219 2010
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.070 GeneticVariation BEFREE APOA5 -1131T > C and S19W single nucleotide polymorphisms (SNP) have been consistently associated with plasma lipid concentration and metabolic syndrome (MetS), alone and in modulation by dietary factors. 19828688 2009
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.070 GeneticVariation BEFREE Gender-modulated impact of apolipoprotein A5 gene (APOA5) -1131T>C and c.56C>G polymorphisms on lipids, dyslipidemia and metabolic syndrome in Turkish adults. 18601598 2008
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.070 GeneticVariation BEFREE Furthermore, the data suggest a different mechanism of APOA5 impact on MetS in Caucasians, as variant c.56C>G (not analyzed in the Japanese study) and not -1131T>C, as in the Japanese subjects, was associated with MetS. 17768309 2007