Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11572325
rs11572325
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0085580
Disease:
Essential Hypertension
0.010 GeneticVariation BEFREE Significant associations were identified among the SNPs rs890293 (OR = 2.17, 95%CI 1.30-3.65), rs2280275 (OR = 1.59, 95%CI 1.10-2.37) and rs11572325 (OR = 1.89, 95%CI 1.22-2.95) and the risk of EH in females from the Kursk population. 30518987 2019
dbSNP: rs11572325
rs11572325
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Moreover, the polymorphisms rs890293, rs2280275, and rs11572325 were found to be significantly associated with hypertension risk in the Belgorod population. 30518987 2019
dbSNP: rs2280275
rs2280275
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Moreover, the polymorphisms rs890293, rs2280275, and rs11572325 were found to be significantly associated with hypertension risk in the Belgorod population. 30518987 2019
dbSNP: rs2280275
rs2280275
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0085580
Disease:
Essential Hypertension
0.010 GeneticVariation BEFREE Significant associations were identified among the SNPs rs890293 (OR = 2.17, 95%CI 1.30-3.65), rs2280275 (OR = 1.59, 95%CI 1.10-2.37) and rs11572325 (OR = 1.89, 95%CI 1.22-2.95) and the risk of EH in females from the Kursk population. 30518987 2019
dbSNP: rs890293
rs890293
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0085580
Disease:
Essential Hypertension
0.010 GeneticVariation BEFREE Significant associations were identified among the SNPs rs890293 (OR = 2.17, 95%CI 1.30-3.65), rs2280275 (OR = 1.59, 95%CI 1.10-2.37) and rs11572325 (OR = 1.89, 95%CI 1.22-2.95) and the risk of EH in females from the Kursk population. 30518987 2019
dbSNP: rs1155002
rs1155002
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0494463
Disease:
Alzheimer Disease, Late Onset
0.010 GeneticVariation BEFREE rs1155002, rs890293 and rs1805192 polymorphism are associated with increased LOAD risk. 27396818 2017
dbSNP: rs890293
rs890293
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0494463
Disease:
Alzheimer Disease, Late Onset
0.010 GeneticVariation BEFREE Participants with GT or TT of rs890293 and CG or GG of rs1805192 genotype have the highest LOAD risk. 27396818 2017
dbSNP: rs890293
rs890293
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE CYP2J2 rs890293 polymorphism is associated with susceptibility to Alzheimer's disease in the Chinese Han population. 25796175 2015
dbSNP: rs2280275
rs2280275
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE The CC genotype of rs2280275 in CYP2J2 gene could be a protective genetic marker of CAD and T allele may be a risk genetic marker of CAD in men of Uygur population in China. 23684773 2013
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: rs890293
rs890293
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Our objective was to investigate CYP2J2 G-50T polymorphism (rs890293) in association with insulin resistance markers and T2DM in a Chinese population. 20140850 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
dbSNP: rs1155002
rs1155002
Entrez Id: 1573
Gene Symbol: CYP2J2
CYP2J2
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE In females, the TT homozygote of rs1155002 seems to be a risk factor for hypertension (p = 0.014). 17286575 2007