Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 25
Gene Symbol: ABL1
ABL1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 283450
Gene Symbol: HECTD4
HECTD4
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 144423
Gene Symbol: GLT1D1
GLT1D1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 55703
Gene Symbol: POLR3B
POLR3B
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 388165
Gene Symbol: UBE2Q2P1
UBE2Q2P1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families. 24778558

2013

Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 84530
Gene Symbol: SRRM4
SRRM4
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 23316
Gene Symbol: CUX2
CUX2
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 113220
Gene Symbol: KIF12
KIF12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 4660
Gene Symbol: PPP1R12B
PPP1R12B
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families. 24778558

2013

Entrez Id: 105370004
Gene Symbol: LINC02463
LINC02463
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 10906
Gene Symbol: TRAFD1
TRAFD1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

Entrez Id: 100507584
Gene Symbol: LINC01016
LINC01016
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

Entrez Id: 30834
Gene Symbol: ZNRD1
ZNRD1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

Entrez Id: 64288
Gene Symbol: ZSCAN31
ZSCAN31
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

Entrez Id: 100129195
Gene Symbol: ZSCAN16-AS1
ZSCAN16-AS1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

Entrez Id: 22895
Gene Symbol: RPH3A
RPH3A
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

Entrez Id: 51809
Gene Symbol: GALNT7
GALNT7
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex. 22319020

2012

Entrez Id: 375612
Gene Symbol: LHFPL3
LHFPL3
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

Entrez Id: 729816
Gene Symbol: DHFRP2
DHFRP2
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

Entrez Id: 283450
Gene Symbol: HECTD4
HECTD4
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. 22751097

2012

Entrez Id: 352962
Gene Symbol: HLA-V
HLA-V
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

Entrez Id: 114821
Gene Symbol: ZBED9
ZBED9
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053

2012

Entrez Id: 6580
Gene Symbol: SLC22A1
SLC22A1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 GeneticVariation GWASDB A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex. 22319020

2012