Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 345
Gene Symbol: APOC3
APOC3
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.400 GeneticVariation LHGDN Therefore, the present study aimed to elucidate the relationship of four single nucleotide polymorphisms (SNPs) in the Apo11q cluster, namely the -75G>A, +83C>T SNPs in the APOA1 gene, the Sac1 SNP in the APOC3 gene and the S19W variant in the APOA5 gene to plasma lipids and CAD in 190 affected sibling pairs (ASPs) belonging to Asian Indian families with a strong CAD history. 18801202

2008
Entrez Id: 345
Gene Symbol: APOC3
APOC3
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.400 Biomarker LHGDN Genetic epistasis in the VLDL catabolic pathway is associated with deleterious variations on triglyceridemia in obese subjects. 17342071

2007
Entrez Id: 345
Gene Symbol: APOC3
APOC3
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.400 GeneticVariation LHGDN The carriership for the -455C variant multiplied the probability of CAD in MS in an allele-specific way and was associated with increased apoC-III and TG levels. 14563827

2003
Entrez Id: 345
Gene Symbol: APOC3
APOC3
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.400 GeneticVariation LHGDN ApoC-III gene polymorphisms and risk of coronary artery disease. 12235176

2002