Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10455872
rs10455872
LPA
0.770 GeneticVariation BEFREE We genotyped the CAD-associated variants at the LPA (rs10455872) and 9p21 loci (rs1333049) in the GeneCAST (Genetics of Calcific Aortic STenosis) Consortium and conducted a meta-analysis for their association with AVS. 30482443

2019

dbSNP: rs10455872
rs10455872
LPA
0.770 GeneticVariation BEFREE The genetic variants of rs3135506 (G), rs10455872 (A) and rs3798220 (G) have low frequency in our population and reflected no association with CAD. 29309886

2018

dbSNP: rs10455872
rs10455872
LPA
G 0.770 GeneticVariation GWASCAT Association analyses based on false discovery rate implicate new loci for coronary artery disease. 28714975

2017

dbSNP: rs10455872
rs10455872
LPA
0.770 GeneticVariation BEFREE We confirmed the association of the LPA rs10455872 with CAD in a large sample of Brazilian patients. 24776095

2014

dbSNP: rs10455872
rs10455872
LPA
0.770 GeneticVariation BEFREE TaqMan SNP genotyping assays were performed to detect the rs6415084, rs3798220 and rs10455872 genotypes in 517 Chinese Han patients with CAD after PCI. 23978127

2013

dbSNP: rs10455872
rs10455872
LPA
0.770 GeneticVariation BEFREE Individuals with the G allele of rs10455872, which represents approximately one in seven patients, have a higher risk of CAD than the majority of the population even after treatment with statins; and therefore represent a vulnerable group requiring an alternative medication in addition to statin treatment. 23903772

2013

dbSNP: rs10455872
rs10455872
LPA
0.770 GeneticVariation BEFREE In conclusion, heritable contributions of LPA rs10455872 and rs3798220 to Lp(a) cholesterol levels and to angiographic CAD were prospectively assessed in this study. 23735648

2013

dbSNP: rs10455872
rs10455872
LPA
0.770 GeneticVariation BEFREE It is unclear whether the LPA variants rs10455872 and rs3798220, which correlate with lipoprotein(a) levels and coronary artery disease (CAD), confer susceptibility predominantly via atherosclerosis or thrombosis. 22898070

2012