rs104894584
|
|
|
0.010 |
GeneticVariation |
BEFREE |
SQT3 variant (linked to the inward rectifier potassium current I <sub>K1</sub>) of SQTS, results from a gain-of-function mutation (Kir2.1 D172N) in the KCNJ2-encoded channels, which is associated with ventricular fibrillation (VF).
|
28812984 |
2017 |
rs10757278
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The aim of the study was to find whether patients carrying polymorphic allele of the rs10757278 polymorphism from 9p21 locus have changed risk of arrhythmia (atrial fibrillation, AF; sustained ventricular tachycardia or ventricular fibrillation, sVT/VF) during acute phase of myocardial infarction.
|
26615606 |
2016 |
rs11720524
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The major C-allele of rs11720524 was present in 64% of the cases and the C/C genotype was significantly associated with VF with an odds ratio (OR) of 1.87 (95% CI: 1.12-3.12; P = 0.017).
|
28085969 |
2017 |
rs12090554
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In a recently published genome-wide association study (GWAS), three single nucleotide polymorphisms (SNPs) (rs2824292, rs1353342, rs12090554) were significantly associated with increased susceptibility for ventricular fibrillation (VF) during acute myocardial infarction (AMI).
|
21574885 |
2011 |
rs121912516
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here we investigated the repeated occurrence of fever-induced polymorphic ventricular tachycardia and ventricular fibrillation in 2 LQT-2 patients with A558P missense mutation in HERG.
|
18551196 |
2008 |
rs1353342
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In a recently published genome-wide association study (GWAS), three single nucleotide polymorphisms (SNPs) (rs2824292, rs1353342, rs12090554) were significantly associated with increased susceptibility for ventricular fibrillation (VF) during acute myocardial infarction (AMI).
|
21574885 |
2011 |
rs188043534
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here, we describe a novel variant of KCR1 (E33D) isolated from a patient with ventricular fibrillation and significant QT prolongation.
|
20950623 |
2011 |
rs192749597
|
|
|
0.010 |
GeneticVariation |
BEFREE |
An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation.
|
30279520 |
2018 |
rs199472708
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In short, using computational model of the ventricle, we predicted that G229D mutation decreased cardiac pumping efficacy and increased the vulnerability of ventricular fibrillation.
|
29488358 |
2018 |
rs199473229
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation.
|
16616735 |
2006 |
rs199473574
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here, we characterized the biophysical properties of a novel Brugada syndrome-associated Nav1.5 mutation, A551T, identified in a proband who was successfully resuscitated from an episode of ventricular fibrillation with sudden collapse.
|
19706159 |
2009 |
rs2824292
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In contrast to the data from the Netherlands, we could not detect a significant association of the rs2824292 locus and risk of VF during AMI in our German cohort.
|
21574885 |
2011 |
rs397514616
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A mutation in TNNC1-encoded cardiac troponin C, TNNC1-A31S, predisposes to hypertrophic cardiomyopathy and ventricular fibrillation.
|
22815480 |
2012 |
rs6125
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The P-selectin gene polymorphism Val168Met: a novel risk marker for the occurrence of primary ventricular fibrillation during acute myocardial infarction.
|
20586826 |
2010 |
rs6795970
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We also find that rs6795970 is associated with a higher risk of heart block (P < 0.05) and a lower risk of ventricular fibrillation (P = 0.01).
|
20062061 |
2010 |
rs9388451
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Marginal associations with VF were also found for rs9388451 in HEY2 gene.
|
28085969 |
2017 |
rs1057518920
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1554093433
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs190140598
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|