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rs1008438
|
|
|
0.010 |
GeneticVariation |
BEFREE |
An analysis was made of the association of two single nucleotide polymorphisms (db rs1008438 -110A/C and db rs1043618 +190 G/C) with circulating and intragranulocytic HSPA1A and the risk of atherosclerosis.
|
22328194 |
2012 |
|
rs1010
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We considered five variants that were associated with coronary heart disease in two studies and confirmed in the Atherosclerosis Risk in Communities study: rs20455 (KIF6), rs3900940 (MYH15), rs7439293 (PALLD), rs2298566 (SNX19), and rs1010 (VAMP8).
|
18073581 |
2007 |
|
rs1020608562
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We aimed to investigate the associations of fractalkine receptor (CX3CR1) V249I, T280M and CCR5-59029 A/G gene polymorphisms in chronic renal failure (CRF) subjects undergoing hemodialysis and to evaluate possible associations of these polymorphisms with hypertension (HT), diabetes mellitus (DM) and atherosclerosis (AS).
|
27118566 |
2016 |
|
rs1022113606
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study, the Thr40Ala and Arg213Gly polymorphic variants of the EC-SOD gene (SOD ( 3 )) were investigated for associations with atherosclerosis and other related factors in 144 subjects with significant atheroma (having one, two, or three major coronary arteries with >50% obstruction, and/or peripheral artery lesions, and/or carotid artery stenosis demonstrated by angiography and echography) and in 150 subjects with no significant atheroma.
|
18726685 |
2008 |
|
rs1042713
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ADRB2 Arg16Gly polymorphism, lung function, and mortality: results from the Atherosclerosis Risk in Communities study.
|
17356698 |
2007 |
|
rs1043618
|
|
|
0.010 |
GeneticVariation |
BEFREE |
An analysis was made of the association of two single nucleotide polymorphisms (db rs1008438 -110A/C and db rs1043618 +190 G/C) with circulating and intragranulocytic HSPA1A and the risk of atherosclerosis.
|
22328194 |
2012 |
|
rs10455872
|
|
|
0.010 |
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 |
|
rs1051931
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We investigated whether Lp-PLA2 activity and PLA2G7 A379V genotype were related to mediators of atherosclerosis in a diabetic study.
|
16438975 |
2006 |
|
rs1056515
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our study identifies a common variant rs1056515 as a genetic marker for CAD and rare variants in LD with rs1056515 leading to decreased expression of RGS5, which contributes to atherosclerosis by impairing endothelial cell function.
|
31605122 |
2019 |
|
rs1061170
|
|
|
0.030 |
GeneticVariation |
BEFREE |
In this study, we examined whether the gene-gene interactions between CRP haplotypes and CFH Tyr402His functional polymorphism exerted an effect on early atherosclerosis.
|
19076828 |
2009 |
|
rs1061170
|
|
|
0.030 |
GeneticVariation |
BEFREE |
In addition, a specific Y402H polymorphism of the complement inhibitor factor H has been found to be associated with the incidence of both AMD and AS.
|
22067048 |
2012 |
|
rs1061170
|
|
|
0.030 |
GeneticVariation |
BEFREE |
We evaluated the association of the Y402H polymorphism with incident coronary heart disease (CHD), incident ischemic stroke, and carotid artery wall thickness (intima-media thickness (IMT)) in the Atherosclerosis Risk in Communities (ARIC) cohort.
|
18292760 |
2008 |
|
rs10757274
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The 9p21 SNP (rs10757274) and multiple risk markers were measured in the Atherosclerosis Risk in Communities Study, and incident coronary disease events were ascertained.
|
22935634 |
2012 |
|
rs10757278
|
|
|
0.010 |
GeneticVariation |
BEFREE |
we tested the hypothesis that the 9p21 risk locus promotes atherosclerosis by examining the association between rs10757278 and coronary artery disease (CAD) severity and progression determined by semi-quantitative angiographic scores.
|
20729229 |
2010 |
|
rs10846744
|
|
|
0.040 |
GeneticVariation |
BEFREE |
Variation in SCARB1 at rs10846744 was significantly associated with CCIMT across racial/ethnic groups in Multi-Ethnic Study of Atherosclerosis.
|
20160195 |
2010 |
|
rs10846744
|
|
|
0.040 |
GeneticVariation |
BEFREE |
The SCARB1 SNP, rs10846744, exerts a major effect on subclinical atherosclerosis and incident cardiovascular disease in humans.
|
22628436 |
2012 |
|
rs10846744
|
|
|
0.040 |
GeneticVariation |
BEFREE |
We identified a potentially novel connection between rs10846744, the immune checkpoint inhibitor lymphocyte activation gene 3 (<i>LAG3</i>), and atherosclerosis.
|
27777974 |
2016 |
|
rs10846744
|
|
|
0.040 |
GeneticVariation |
BEFREE |
SCARB1 rs10846744 is significantly associated with Lp-PLA2 activity, atherosclerosis, and CVD events, but Lp-PLA2 activity is not a mediator in the association of rs10846744 with cIMT in MESA.
|
30289950 |
2018 |
|
rs11209026
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Analysis of the association between IL-23R rs11209026 polymorphism and incidence of atherosclerosis.
|
26261042 |
2015 |
|
rs1122608
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Further studies were used to identify the most likely mechanism by which rs1122608 regulates atherosclerosis.
|
24190014 |
2014 |
|
rs1126478
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The relationships among lactoferrin genotypes, lactoferrin concentrations, and clinical factors on the risk for atherosclerosis are not fully understood, but the G allele of rs1126478 seems to have a detrimental effect in a European population.
|
22406253 |
2012 |
|
rs112735431
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The p.R4810K heterozygous variant was identified in 5 patients, including 3 patients with atherosclerosis, 1 patient with Graves disease, and 1 patient with rheumatoid arthritis; it was also observed in one control.
|
28063898 |
2017 |
|
rs1130864
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We genotyped 3 tag single nucleotide polymorphisms (SNPs) [+1444T>C (rs1130864); +2303G>A (rs1205) and +4899T>G (rs 3093077)] in the CRP gene and assessed CRP and carotid intima-media thickness (CIMT), a structural marker of atherosclerosis, in 4941 men and women aged 50-74 (mean 61) years (the Whitehall II Study).
|
18714381 |
2008 |
|
rs1130864
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We concluded that rs3091244, rs1130864 and the T-T-G haplotype are genetic markers for elevated basal CRP levels. rs1800947 and the C-C-C haplotype appear to be susceptibility markers for atherosclerosis, but this requires confirmation.
|
16832152 |
2006 |
|
rs1137100
|
|
|
0.020 |
GeneticVariation |
BEFREE |
To evaluate the potential contribution of LEPrs2167270(19 G/A), LEPRrs1137100(326 A/G) and ADIPOQrs1501299(276 G/T) gene polymorphisms in psoriasis susceptibility and their influence in epicardial adipose tissue and abdominal visceral fat volume and subclinical atherosclerosis in severe psoriasis patients.
|
26123401 |
2015 |