|
rs4977574
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Neither education nor physical activity-leve</span>ls modified the associated risk of CAD, ischemic stroke and CVD mortality conferred by rs4977574.
|
24465769 |
2014 |
|
rs4977574
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Our results indicate that rs4977574 interacts with vegetable and wine intake to affect the incidence of CVD, and suggest that an interaction may exist between environmental risk factors and rs4977574 on known risk markers of CVD.
|
25551366 |
2014 |
|
rs4977574
|
|
|
0.030 |
GeneticVariation |
BEFREE |
rs4977574 on chromosome 9p21 was genotyped in 24 777 subjects from the Malmö Diet and Cancer study who were free from CVD prior to the baseline examination.
|
23480785 |
2013 |
|
rs1333049
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Candidate genes, including SNP markers rs1333049 (CDKN2B, 9p21.3), rs17465637 (MIA3, 1q41) and rs501120 (CXCL12, 10q11.21), were genotyped to analyze the association with future CVD.
|
31804579 |
2019 |
|
rs10757274
|
|
|
0.020 |
GeneticVariation |
BEFREE |
This study aimed to confirm the effect of common putative CVD-associated gene variants (FTO rs17817449, KIF6 rs20455, 9p21 rs10757274 and 2q36.3 rs2943634) on CVD manifestation, and determine whether this effect differs between younger (< 50 years) and older CVD patients.
|
26772723 |
2016 |
|
rs10757274
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Study subjects were followed up for development of SCD, and genotypes for rs10757274 were determined for 492 sudden and/or arrhythmic deaths and 1460 controls matched for age, sex, cohort, history of cardiovascular disease, and follow-up time.
|
19901189 |
2009 |
|
rs1333049
|
|
|
0.020 |
GeneticVariation |
BEFREE |
We studied the rs1333049 polymorphism located on chromosome 9p21 in a cohort of 769 individuals who participated in the Bruneck study with long-term follow-up data on carotid atherosclerosis measured by high-resolution duplex ultrasound and incident cardiovascular disease.
|
18652946 |
2008 |
|
rs3217992
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ANRIL SNPs rs133049 and rs3217992 were not associated with severe periodontitis or history of CVD in CV patients.
|
29732560 |
2018 |
|
rs10116277
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In conclusion, results do not support a role of rs10116277 or rs1537375 SNPs in CVD risk in Spanish RA patients.
|
24498997 |
2013 |
|
rs1537375
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In conclusion, results do not support a role of rs10116277 or rs1537375 SNPs in CVD risk in Spanish RA patients.
|
24498997 |
2013 |
|
rs10757278
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The risk variant on chromosome 9, tagged by rs10757278, is associated with coronary heart disease in the Belgian population, but not with isolated CVD.
|
19319159 |
2009 |