Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.430 GeneticVariation disease GWASCAT A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. 26343387 2015
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.430 GeneticVariation disease BEFREE Genome-wide association studies have described an association between MIA3 rs17465637 A/C polymorphisms and coronary artery disease and myocardial infarction. 22577832 2012
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.430 GeneticVariation disease BEFREE Our results establish two SNPs, rs17465637 in MIA3 and rs599839 near SORT1 as significant risk factors for MI in the American Genebank Caucasian population. 21463265 2011
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.430 GeneticVariation disease BEFREE In addition to correspond with such isolated evidence of association with MI, the present study identified specific haplotypes capturing the risk-related variation in the entire MIA3 region. 21264445 2011
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.430 Biomarker disease CTD_human Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609 2009
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.430 GeneticVariation disease GWASCAT Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609 2009
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.430 GeneticVariation disease GWASDB Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609 2009