Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs693
rs693
0.710 GeneticVariation BEFREE To examine the association between apolipoprotein B (ApoB) XbaI polymorphisms (rs693) and coronary heart disease (CHD) risk among the Han Chinese population by systematically analyzing multiple independent studies. 27172140

2016

dbSNP: rs693
rs693
0.710 GeneticVariation GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282

2011

dbSNP: rs1042031
rs1042031
0.010 GeneticVariation BEFREE The study was carried out to examine the association between apolipoprotein B (ApoB) EcoRI polymorphism (E<sup>-</sup> vs. E<sup>+</sup>) (rs1042031) and coronary heart disease (CHD) risk by systematically analyzing multiple independent studies. 27637205

2016

dbSNP: rs749903604
rs749903604
0.010 GeneticVariation BEFREE We investigated the relationship between the single nucleotide polymorphism at position -148 in the beta-fibrinogen gene promoter (beta - 148C/T), blood fibrinogen levels, and risk of myocardial infarction (MI) in sufficiently large numbers of coronary disease cases to reliably address this question. 16870675

2006

dbSNP: rs5742904
rs5742904
0.010 GeneticVariation BEFREE None of the 274 individuals in the coronary heart disease (CHD) groups was found to be a carrier of the apoB allele Arg3500----Gln, previously shown to be associated with an apoB protein defective in binding to the low density lipoprotein receptor (LDL-R). 1346774

1992