|
rs3798220
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Aim was to estimate the genotypic distribution and risk allele frequencies of 13 Coronary Artery Disease (CAD) risk Single Nucleotide Polymorphisms in loci identified by the CARDIoGRAMplusC4D consortium namely MIA3 rs17465637; 9p21 rs10757274; CXCL12 rs1746048; APOA5 rs662799; APOB rs1042031; LPA rs3798220; LPA 10455872; MRAS rs9818870; LPL rs328; SORT1 rs646776; PCSK9 rs11591147; APOE rs429358; APOE rs7412 in Pakistani PCAD patients and controls.
|
28705542 |
2019 |
|
rs3798220
|
|
|
0.090 |
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 |
|
rs3798220
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Both allelic and genotypic associations of rs964184, rs2895811 and rs3798220 with CAD were significant, regardless of adjustment for covariates of gender, age, hypertension, type 2 diabetes, blood lipid profiles and smoking.
|
26740236 |
2016 |
|
rs3798220
|
|
|
0.090 |
GeneticVariation |
BEFREE |
The variant allele of rs379</span>8220 in the apolipoprotein(a) gene (LPA) is used to assess the risk for coronary artery disease (CAD) in Europeans, where it is associated with short alleles of the Kringle IV-2 (KIV-2) copy number variation (CNV) and high lipoprotein(a) (Lp(a)) concentrations.
|
26302166 |
2015 |
|
rs3798220
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Our data did not support a relationship between genetic LPA variants (rs6415084 and rs3798220) and subsequent cardiovascular events after PCI in Chinese Han CAD patients.
|
23978127 |
2013 |
|
rs3798220
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Rs10455872 strongly predicted prevalent CAD (per allele OR 1.43, 95% CI 1.07 to 1.91, p = 0.0172); the effect size for the rare rs3798220 variant was similar (dominant OR 1.47, 95% CI 0.81 to 2.67, p = 0.20), but power was limited to demonstrate significance.
|
23735648 |
2013 |
|
rs3798220
|
|
|
0.090 |
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 |
|
rs3798220
|
|
|
0.090 |
GeneticVariation |
BEFREE |
The LPA I4399M (rs3798220) single nucleotide polymorphism (SNP) is associated with increased plasma levels of Lp(a) and advanced coronary artery disease (CAD).
|
19880117 |
2010 |
|
rs3798220
|
|
|
0.090 |
GeneticVariation |
BEFREE |
We found 1 SNP that was associated with severe CAD: LPA I4399M (rs3798220).
|
17569884 |
2007 |