Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 440823
Gene Symbol: MIAT
MIAT 		0.500 GeneticVariation disease GWASDB These results indicate that the altered expression of MIAT by the SNP may play some role in the pathogenesis of MI. 17066261 2006
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1 		0.490 GeneticVariation disease GWASDB Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609 2009
Entrez Id: 8315
Gene Symbol: BRAP
BRAP 		0.450 GeneticVariation disease GWASDB A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese. 24916648 2015
Entrez Id: 8315
Gene Symbol: BRAP
BRAP 		0.450 GeneticVariation disease GWASDB SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population. 21107343 2011
Entrez Id: 375056
Gene Symbol: MIA3
MIA3 		0.430 GeneticVariation disease GWASDB Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609 2009
Entrez Id: 55759
Gene Symbol: WDR12
WDR12 		0.410 GeneticVariation disease GWASDB Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609 2009
Entrez Id: 6387
Gene Symbol: CXCL12
CXCL12 		0.400 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1 		0.180 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 100048912
Gene Symbol: CDKN2B-AS1
CDKN2B-AS1 		0.150 GeneticVariation disease GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679 2007
Entrez Id: 100048912
Gene Symbol: CDKN2B-AS1
CDKN2B-AS1 		0.150 GeneticVariation disease GWASDB Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609 2009
Entrez Id: 1284
Gene Symbol: COL4A2
COL4A2 		0.140 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 3609
Gene Symbol: ILF3
ILF3 		0.140 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A 		0.130 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 3909
Gene Symbol: LAMA3
LAMA3 		0.120 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 3663
Gene Symbol: IRF5
IRF5 		0.110 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 8943
Gene Symbol: AP3D1
AP3D1 		0.110 GeneticVariation disease GWASDB A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese. 24916648 2015
Entrez Id: 23228
Gene Symbol: PLCL2
PLCL2 		0.110 GeneticVariation disease GWASDB A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese. 24916648 2015
Entrez Id: 79109
Gene Symbol: MAPKAP1
MAPKAP1 		0.110 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 51062
Gene Symbol: ATL1
ATL1 		0.110 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 3699
Gene Symbol: ITIH3
ITIH3 		0.110 GeneticVariation disease GWASDB Furthermore, we found expression of the ITIH3 protein in the vascular smooth muscle cells and macrophages in the human atherosclerotic lesions, suggesting ITIH3 SNP to be a novel genetic risk factor of MI. 17211523 2007
Entrez Id: 6597
Gene Symbol: SMARCA4
SMARCA4 		0.110 GeneticVariation disease GWASDB Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609 2009
Entrez Id: 4043
Gene Symbol: LRPAP1
LRPAP1 		0.110 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 6305
Gene Symbol: SBF1
SBF1 		0.100 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 3340
Gene Symbol: NDST1
NDST1 		0.100 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
Entrez Id: 421
Gene Symbol: ARVCF
ARVCF 		0.100 GeneticVariation disease GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011