Disease: Myocardial Infarction ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2271800
rs2271800
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0027051
Disease:
Myocardial Infarction 		0.010 GeneticVariation BEFREE The present results indicate that MI is associated with the CC genotype of rs2271800 in the human CYP2J2 gene. 20597138 2010
dbSNP: rs10889160
rs10889160
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0027051
Disease:
Myocardial Infarction 		0.010 GeneticVariation BEFREE Two intronic CYP2J2 tag-single nucleotide polymorphisms, rs10889160 and rs11572325 were associated with an increased risk of myocardial infarction (odds ratio: 1.24, 95% confidence interval: 1.07-1.43, P=0.004, q=0.090, and odds ratio: 1.27, 95% confidence interval: 1.08-1.51, P=0.006, q=0.090, respectively). 18496133 2008
dbSNP: rs11572325
rs11572325
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0027051
Disease:
Myocardial Infarction 		0.010 GeneticVariation BEFREE Two intronic CYP2J2 tag-single nucleotide polymorphisms, rs10889160 and rs11572325 were associated with an increased risk of myocardial infarction (odds ratio: 1.24, 95% confidence interval: 1.07-1.43, P=0.004, q=0.090, and odds ratio: 1.27, 95% confidence interval: 1.08-1.51, P=0.006, q=0.090, respectively). 18496133 2008