INSIG2, insulin induced gene 2, 51141

N. diseases: 45; N. variants: 8
Disease: Metabolic Syndrome X ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.030 GeneticVariation disease BEFREE We hypothesized that the association between dietary patterns and components of the metabolic syndrome could be modified by INSIG2 variants. 22968099 2013
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.030 GeneticVariation disease BEFREE In addition, haplotype analysis showed that the C-C-C haplotype of rs11123469-rs10185316- rs1559509 of the INSIG2 gene significantly increased the risk of MetS (P=0.0023). 20877301 2012
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.030 GeneticVariation disease BEFREE Subjects were genotyped for both the APOC3 -455T>C and INSIG2 rs7566605 polymorphisms, and classified for the presence or absence of MetS (NCEP ATP III and IDF definitions). 18096054 2007