INS, insulin, 3630

N. diseases: 405; N. variants: 37
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.310 GeneticVariation phenotype LHGDN Polymorphisms in candidate genes for type 2 diabetes mellitus in a Mexican population with metabolic syndrome findings. 14693412 2004
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.310 Biomarker phenotype CTD_human Decreased PLTP mass but elevated PLTP activity linked to insulin resistance in HTG: effects of bezafibrate therapy. 12754275 2003