AGTR1, angiotensin II receptor type 1, 185

N. diseases: 440; N. variants: 33
Disease: Coronary Arteriosclerosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3772622
rs3772622
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0010054
Disease:
Coronary Arteriosclerosis 		0.010 GeneticVariation BEFREE AGTR1 rs3772622 gene polymorphism increase the risk of nonalcoholic fatty liver disease patients suffer coronary artery disease in Northern Chinese Han population. 27342049 2016
dbSNP: rs5186
rs5186
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0010054
Disease:
Coronary Arteriosclerosis 		0.010 GeneticVariation BEFREE Association study of angiotensin II type 1 receptor: A1166C (rs5186) polymorphism with coronary heart disease using systematic meta-analysis. 22645060 2013
dbSNP: rs150629733
rs150629733
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0010054
Disease:
Coronary Arteriosclerosis 		0.010 GeneticVariation BEFREE The p22 phox A640G gene polymorphism but not the C242T gene variation is associated with coronary heart disease in younger individuals. 10488959 1999
dbSNP: rs553350297
rs553350297
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0010054
Disease:
Coronary Arteriosclerosis 		0.010 GeneticVariation BEFREE Our observations allow the assumption that the p22 phox A640G gene polymorphism is independently associated with the presence and extent of coronary artery disease. 10488959 1999
dbSNP: rs5182
rs5182
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0010054
Disease:
Coronary Arteriosclerosis 		0.010 GeneticVariation BEFREE In a preliminary study we found no association between the distribution of the C/T573 polymorphic site and cardiovascular disease, such as essential hypertension (n = 20) coronary artery disease (n = 16) hypertrophic cardiomyopathy (n = 12) or dilated cardiomyopathy (n = 21). 7713099 1994