Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518920
rs1057518920
DSP
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554093433
rs1554093433
T 0.700 CausalMutation CLINVAR

dbSNP: rs190140598
rs190140598
T 0.700 CausalMutation CLINVAR

dbSNP: rs192749597
rs192749597
0.010 GeneticVariation BEFREE An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation. 30279520

2018

dbSNP: rs199472708
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

dbSNP: rs104894584
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

dbSNP: rs11720524
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

dbSNP: rs9388451
rs9388451
0.010 GeneticVariation BEFREE Marginal associations with VF were also found for rs9388451 in HEY2 gene. 28085969

2017

dbSNP: rs10757278
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

dbSNP: rs397514616
rs397514616
0.010 GeneticVariation BEFREE A mutation in TNNC1-encoded cardiac troponin C, TNNC1-A31S, predisposes to hypertrophic cardiomyopathy and ventricular fibrillation. 22815480

2012

dbSNP: rs12090554
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

dbSNP: rs1353342
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

dbSNP: rs188043534
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

dbSNP: rs2824292
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

dbSNP: rs6125
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

dbSNP: rs6795970
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

dbSNP: rs199473574
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

dbSNP: rs121912516
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

dbSNP: rs199473229
rs199473229
0.010 GeneticVariation BEFREE A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation. 16616735

2006