Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26154
Gene Symbol: ABCA12
ABCA12 		0.100 Biomarker phenotype HPO
Entrez Id: 368
Gene Symbol: ABCC6
ABCC6 		0.100 Biomarker phenotype HPO
Entrez Id: 64240
Gene Symbol: ABCG5
ABCG5 		0.100 Biomarker phenotype HPO
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8 		0.100 Biomarker phenotype HPO
Entrez Id: 28976
Gene Symbol: ACAD9
ACAD9 		0.100 Biomarker phenotype HPO
Entrez Id: 33
Gene Symbol: ACADL
ACADL 		0.100 Biomarker phenotype HPO
Entrez Id: 37
Gene Symbol: ACADVL
ACADVL 		0.100 Biomarker phenotype HPO
Entrez Id: 98
Gene Symbol: ACYP2
ACYP2 		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: 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: 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: 10142
Gene Symbol: AKAP9
AKAP9 		0.100 Biomarker phenotype HPO
Entrez Id: 207
Gene Symbol: AKT1
AKT1 		0.100 Biomarker phenotype HPO
Entrez Id: 144245
Gene Symbol: ALG10B
ALG10B 		0.100 Biomarker phenotype HPO
Entrez Id: 287
Gene Symbol: ANK2
ANK2 		0.100 Biomarker phenotype HPO
Entrez Id: 8906
Gene Symbol: AP1G2
AP1G2 		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: 338
Gene Symbol: APOB
APOB 		0.100 Biomarker phenotype HPO
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: 466
Gene Symbol: ATF1
ATF1 		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: 9031
Gene Symbol: BAZ1B
BAZ1B 		0.100 Biomarker phenotype HPO
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: 775
Gene Symbol: CACNA1C
CACNA1C 		0.410 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: 775
Gene Symbol: CACNA1C
CACNA1C 		0.410 Biomarker phenotype HPO
Entrez Id: 775
Gene Symbol: CACNA1C
CACNA1C 		0.410 Biomarker phenotype GENOMICS_ENGLAND Emerging therapeutic targets in the short QT syndrome. 29697308 2018
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1 		0.110 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: 781
Gene Symbol: CACNA2D1
CACNA2D1 		0.110 Biomarker phenotype HPO