Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4762
rs4762
AGT
0.020 GeneticVariation BEFREE Polymorphisms of AGT Met235Thr and AGT Thr174Met genes are able to mark increased or reduced odds ratio of circumflex artery as culprit artery in STEMI. 22475523

2012

dbSNP: rs699
rs699
AGT
0.020 GeneticVariation BEFREE Polymorphisms of AGT Met235Thr and AGT Thr174Met genes are able to mark increased or reduced odds ratio of circumflex artery as culprit artery in STEMI. 22475523

2012

dbSNP: rs4762
rs4762
AGT
0.020 GeneticVariation BEFREE The most powerful predictive value for STEMI was represented by the Thr/Met genotype and the Met174 allele of the AGT Thr174Met gene polymorphism. 21657802

2011

dbSNP: rs699
rs699
AGT
0.020 GeneticVariation BEFREE A total of 100 patients (mean age 57 ± 10 years [range 31-76 years]; 21% women) with diagnosed STEMI and a control group consisting of 95 healthy volunteers (mean age 38 ± 11 years [range 17-60 years]; 20% women) were investigated for the AGTR1 1166A/C polymorphism and two variants of AGT (Met235Thr and Thr174Met). 21657802

2011

dbSNP: rs7895833
rs7895833
0.010 GeneticVariation BEFREE Genotyping of the three single-nucleotide polymorphisms (rs7895833 A > G in the promoter region, rs7069102 C > G in intron 4, and rs2273773 C > T in exon 5) in <i>SIRT1</i> gene was performed in 108 consecutive patients (87.0% were men with a mean age of 40.74 ± 3.82 years) suffering from ST-elevation myocardial infarction at the age of ≤45 and 91 control subjects. 31143479

2019

dbSNP: rs11720524
rs11720524
0.010 GeneticVariation BEFREE Of the 27 candidate SNPs, one SNP (rs11720524) located in intron 1 of SCN5A which was previously associated with SCD was significantly associated with VF caused by first STEMI. 28085969

2017

dbSNP: rs2228145
rs2228145
0.010 GeneticVariation BEFREE The rs2228145 polymorphism of IL6R was not significantly associated with long-term mortality after STEMI. 28144260

2017

dbSNP: rs10757278
rs10757278
0.010 GeneticVariation BEFREE SNP rs10757278 is not linked with sVT/VF in acute phase of STEMI. 26615606

2016

dbSNP: rs2107595
rs2107595
0.010 GeneticVariation BEFREE Subsequent genotype-phenotype analyses observed the significant correlations of SNP rs2107595 with HDAC9 mRNA expression and plasma HDAC9 levels in controls and patients with NSTEMI and STEMI. 27494404

2016

dbSNP: rs662
rs662
0.010 GeneticVariation BEFREE We investigated the association of rs662 and rs854560 SNPs of the PON1 gene with 5-year mortality in patients with ST-elevation myocardial infarction (STEMI) treated invasively. 25155309

2016

dbSNP: rs854560
rs854560
0.010 GeneticVariation BEFREE We investigated the association of rs662 and rs854560 SNPs of the PON1 gene with 5-year mortality in patients with ST-elevation myocardial infarction (STEMI) treated invasively. 25155309

2016

dbSNP: rs1801133
rs1801133
0.010 GeneticVariation BEFREE The rs1801133 polymorphism of methylenetetrahydrofolate reductase gene- the association with 5-year survival in patients with ST-elevation myocardial infarction. 22440940

2012

dbSNP: rs1217691063
rs1217691063
0.010 GeneticVariation BEFREE The TT genotype from the C677T of 5,10 MTHFR gene is not an independent risk factor for STEMI in the Mexican population. 20637366

2010

dbSNP: rs1799983
rs1799983
0.010 GeneticVariation BEFREE The Glu298ASP polymorphism of the endothelial nitric oxide synthase gene is associated with premature ST elevation myocardial infarction in Mexican population. 20083095

2010

dbSNP: rs1042713
rs1042713
0.010 GeneticVariation BEFREE In this study, we aimed to investigate the possible relationship between Ser49Gly and Arg389Gly polymorphisms of the ADRB1 and Arg16Gly and Gln27Glu polymorphisms of the ADRB2 gene with ST elevation myocardial infarction (MI) in a Turkish population. 19623647

2009

dbSNP: rs1042714
rs1042714
0.010 GeneticVariation BEFREE For the ADRB2 Gln27Glu polymorphism, subjects having one or two copies of the Glu27 allele showed a decreased risk of MI compared with Gln27 homozygote subjects (OR=0.48, 95% CI=0.24-0.94, P=0.03). 19623647

2009

dbSNP: rs1801252
rs1801252
0.010 GeneticVariation BEFREE In this study, we aimed to investigate the possible relationship between Ser49Gly and Arg389Gly polymorphisms of the ADRB1 and Arg16Gly and Gln27Glu polymorphisms of the ADRB2 gene with ST elevation myocardial infarction (MI) in a Turkish population. 19623647

2009

dbSNP: rs1801253
rs1801253
0.010 GeneticVariation BEFREE These results suggest that the Arg389Gly and Gln27Glu polymorphisms may be associated with an altered risk of MI in this Turkish population. 19623647

2009