Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3606
Gene Symbol: IL18
IL18 		0.010 GeneticVariation phenotype LHGDN IL-18 promoter -137G/C polymorphism, which regulates the expression of IL-18, is an important predictor of SCD from any cause as well as SCD in patients with and without underlying CHD. 17765248 2008
Entrez Id: 783
Gene Symbol: CACNB2
CACNB2 		0.010 GeneticVariation phenotype LHGDN Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death. 17224476 2007
Entrez Id: 3990
Gene Symbol: LIPC
LIPC 		0.010 GeneticVariation phenotype LHGDN Age-dependent association between hepatic lipase gene C-480T polymorphism and the risk of pre-hospital sudden cardiac death: the Helsinki Sudden Death Study. 16793047 2007
Entrez Id: 154
Gene Symbol: ADRB2
ADRB2 		0.010 Biomarker phenotype LHGDN In this study, 4441 white and 808 black Cardiovascular Health Study (CHS) participants were followed up prospectively for SCD and genotyped for B2AR Gly16Arg and Gln27Glu polymorphisms. 16618831 2006
Entrez Id: 9475
Gene Symbol: ROCK2
ROCK2 		0.010 AlteredExpression phenotype LHGDN Remnant lipoproteins from patients with sudden cardiac death enhance coronary vasospastic activity through upregulation of Rho-kinase. 15044207 2004
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		0.010 GeneticVariation phenotype LHGDN In this study of AMI patients, SCD was not related to polymorphisms in the KCNJ11 gene. 14871556 2004
Entrez Id: 6093
Gene Symbol: ROCK1
ROCK1 		0.010 AlteredExpression phenotype LHGDN Remnant lipoproteins from patients with sudden cardiac death enhance coronary vasospastic activity through upregulation of Rho-kinase. 15044207 2004
Entrez Id: 151
Gene Symbol: ADRA2B
ADRA2B 		0.010 GeneticVariation phenotype LHGDN Middle-aged white men carrying the DD genotype of the alpha(2B)-AR have a significantly increased risk for SCD and AMI, especially before the age of 55 years. 12535806 2003
Entrez Id: 25791
Gene Symbol: NGEF
NGEF 		0.100 GeneticVariation phenotype GWASCAT A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. 30169657 2018
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		0.100 GeneticVariation phenotype GWASDB Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease. 23593153 2013
Entrez Id: 22891
Gene Symbol: ZNF365
ZNF365 		0.100 GeneticVariation phenotype GWASDB Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease. 23593153 2013
Entrez Id: 22930
Gene Symbol: RAB3GAP1
RAB3GAP1 		0.100 GeneticVariation phenotype GWASDB Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease. 23593153 2013
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 123099
Gene Symbol: DEGS2
DEGS2 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 2099
Gene Symbol: ESR1
ESR1 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 143
Gene Symbol: PARP4
PARP4 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 221079
Gene Symbol: ARL5B
ARL5B 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 51196
Gene Symbol: PLCE1
PLCE1 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 162333
Gene Symbol: MARCHF10
MARCHF10 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 151126
Gene Symbol: ZNF385B
ZNF385B 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 29994
Gene Symbol: BAZ2B
BAZ2B 		0.100 GeneticVariation phenotype GWASCAT Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. 21738491 2011
Entrez Id: 84441
Gene Symbol: MAML2
MAML2 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 2890
Gene Symbol: GRIA1
GRIA1 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 374491
Gene Symbol: TPTE2P6
TPTE2P6 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
Entrez Id: 1143
Gene Symbol: CHRNB4
CHRNB4 		0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011