SLC22A3, solute carrier family 22 member 3, 6581

N. diseases: 154; N. variants: 30
Disease: Coronary heart disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.160 GeneticVariation disease BEFREE PHACTR1 and SLC22A3 gene polymorphisms are associated with reduced coronary artery disease risk in the male Chinese Han population. 27893421 2017
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.160 GeneticVariation disease BEFREE Functional Variant in the SLC22A3-LPAL2-LPA Gene Cluster Contributes to the Severity of Coronary Artery Disease. 27417586 2016
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.160 GeneticVariation disease BEFREE Our findings might indicate a negative feedback mechanism against inflammatory response by which SLC22A3 polymorphisms decreased the risk of CHD. 25561729 2015
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.160 GeneticVariation disease GWASCAT Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325 2014
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.160 GeneticVariation disease BEFREE Relatively low numbers of kringle 4 type 2 repeats in apolipoprotein(a) and specific haplotypes of the SLC22A3-LPAL2-LPA region on chromosome 6 are associated with an increased risk of coronary disease. 23278389 2013
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.160 GeneticVariation disease BEFREE Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study. 23036009 2012
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.160 GeneticVariation disease GWASCAT Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. 19198611 2009
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.160 GeneticVariation disease BEFREE Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. 19198611 2009