rs10757278
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found that the rs10757278 GG genotype was significantly associated with recurrent angina compared with the AA and AG genotypes (P = 0.013).
|
23454037 |
2013 |
rs1108580
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The minor alleles of rs1611115 and rs1108580 were associated with sympathetic phenotypes, including angina pectoris.
|
25326128 |
2014 |
rs1611115
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The minor alleles of rs1611115 and rs1108580 were associated with sympathetic phenotypes, including angina pectoris.
|
25326128 |
2014 |
rs4646156
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The AA genotype of rs4646156 had a 7.81× higher risk of severe angina pectoris in women (OR = 7.81, p = 0.05).
|
23077079 |
2013 |
rs10911021
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Over a median of 9.6 years of follow-up, the risk (C) allele for GLUL rs10911021 was significantly associated with the primary composite end point of death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for angina among individuals with no history of cardiovascular disease (CVD) at baseline using additive genetic models (hazard ratio 1.17 [95% CI 1.01-1.36]; P = 0.032).
|
26395743 |
2016 |
rs281432
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Multivariate analysis revealed that ICAM-1 SNP rs281432 CC/CG [p=0.016; odds ratio (OR): 2.56, 95% confidence interval (CI): 1.19-5.56], male gender (p=0.018; OR: 1.66, 95% CI: 1.09-2.51), aspirin use in the past 7 days (p=0.001; OR: 2.05, 95% CI: 1.33-3.14), hypertension (p<0.001; OR: 2.15, 95% CI: 1.42-3.25), serum cardiac troponin I elevation (p<0.001; OR: 2.14, 95% CI: 1.47-3.24) and severe angina in recent 24 hours (p=0.001; OR: 1.97, 95% CI: 1.31- 2.95) increase the risk of CAD.
|
26078712 |
2015 |
rs7667298
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In VEGFR-2 -271A>G (rs7667298), the GG carriers had a lower proportion of target lesion revascularization and angina pectoris in contrast to the AA + AG carriers (all P < 0.05).
|
25738571 |
2017 |
rs4977574
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In this follow-up study, rs4977574, a tag SNP at chromosome 9p21, was shown to be associated with cardiovascular mortality in Taiwanese patients with angina pectoris but no coronary lesions.
|
26426617 |
2015 |
rs3742264
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In France, Thr/Thr carriers of the Ala147Thr polymorphism were significantly more frequent in cases than in controls (p = 0.01) leading to a relative risk of angina pectoris of 2.7 (95%CI 1.2-5.8).
|
12624641 |
2003 |
rs5443
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Effects of lifestyle modification on the progression of coronary atherosclerosis, autonomic function, and angina--the role of GNB3 C825T polymorphism.
|
16569552 |
2006 |
rs1064794259
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A novel homozygous 1439 C-->T mutation of the LDL-R gene was detected in the patient and his family.ECG showed atypical angina pectoris.
|
18701038 |
2008 |
rs770696696
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A novel homozygous 1439 C-->T mutation of the LDL-R gene was detected in the patient and his family.ECG showed atypical angina pectoris.
|
18701038 |
2008 |
rs146243018
|
|
|
0.010 |
GeneticVariation |
BEFREE |
3 potentially pathogenic variants were identified: c.-77G>A in <i>GATA2</i>, p.Ala343Thr (rs370588269) in <i>GATA4</i>, and p.Pro555Ala (rs146243018) in <i>GATA6</i> Multivariate analyses showed that angina was more frequent in patients carrying sarcomeric and GATA rare variants (55% vs 23.2% in non-carriers of GATA rare variants, OR (95% CI) 7.12 (1.23 to 41.27), p=0.029).
|
28381408 |
2017 |
rs370588269
|
|
|
0.010 |
GeneticVariation |
BEFREE |
3 potentially pathogenic variants were identified: c.-77G>A in <i>GATA2</i>, p.Ala343Thr (rs370588269) in <i>GATA4</i>, and p.Pro555Ala (rs146243018) in <i>GATA6</i> Multivariate analyses showed that angina was more frequent in patients carrying sarcomeric and GATA rare variants (55% vs 23.2% in non-carriers of GATA rare variants, OR (95% CI) 7.12 (1.23 to 41.27), p=0.029).
|
28381408 |
2017 |
rs114303883
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1481200467
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555512158
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555513085
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555514089
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555514467
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555520991
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs199473620
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs2856597
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs28939702
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs60791294
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|