rs699, AGT

N. diseases: 134
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE In addition, the T235M polymorphism in the AGT product is associated with an increased risk of essential hypertension in multiple populations, making AGT a good example of a quantitative-trait locus underlying susceptibility to a common disease. 11731937 2002
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE These results support the linkage of essential hypertension to the angiotensinogen locus but do not indicate a specific role for the M235T variant. 9314412 1997
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE To determine whether carotid artery stiffness was increased in patients with untreated essential hypertension who are homozygous for the T allele of the M235T polymorphism of the angiotensinogen (AGT) gene and in mutant mice carrying three copies of the angiotensinogen (Agt) gene. 15201545 2004
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE A common variant at codon 235 of the angiotensinogen gene with methionine to threonine amino acid substitution (AGT M235T) has been reported as a genetic risk for essential hypertension. 11230286 2001
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE Meta-analysis of the association of 4 angiotensinogen polymorphisms with essential hypertension: a role beyond M235T? 18227406 2008
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE Two molecular variants of the angiotensinogen gene, one encoding threonine instead of methionine at position 235 (M235T) and the other encoding methionine rather than threonine at position 174 (T174M), were also tested for possible association with essential hypertension. 8177268 1994
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE The molecular variant M235T, but not T174M, of the AGT gene is associated significantly with essential hypertension in this Taiwanese population. 9218179 1997
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE The angiotensinogen (AGT) gene M235T variant is associated with essential hypertension and elevated plasma AGT concentrations, although the underlying mechanisms are unknown. 9403548 1997
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE Furthermore, variation in the number of M235T alleles did not make a significant contribution to predicting the probability of having essential hypertension, either alone or in conjunction with other predictor variables. 7649545 1995
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE The present meta-analysis suggests that AGT M235T and ACE I/D modulate the risk of essential hypertension in Han Chinese population. 20087216 2010
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE Several studies in different populations link Threonine instead of methionine at position 235 (M235T) and Methinine instead of threonine at position 174 (T174M) polymorphisms with essential hypertension. 18404605 2008
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE Gender-related association of AGT gene variants (M235T and T174M) with essential hypertension--a case-control study. 22148914 2012
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE The M235T polymorphism of the angiotensinogen gene (AGT) is associated with an increased risk of primary hypertension, which may then lead to progressive renal disease. 12164881 2002
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE Our single-locus analysis revealed that except for a marginal, significant association of A-20C allele distribution, no significant association between genotype and allele distributions of the A-20C, A-6G, or M235T polymorphism of AGT and essential hypertension was found. 18250562 2007
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE Recently, we reported evidence for genetic linkage between human essential hypertension and the angiotensinogen gene (AGT) and an association with a common molecular variant of this gene (methionine 235 --> threonine or T235). 8728297 1996
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE Although polymorphisms in renin-angiotensin-aldosterone (RAA) system genes for angiotensinogen (AGT M235T), angiotensin-converting enzyme (ACE I/D), angiotensin II type 1 receptor (AT1 A/C1166), and aldosterone synthase (CYP11B2-344T/C) have been major targets for genetic investigation in association with essential hypertension (EH), the influence of these genetic factors is still to be determined. 17190732 2007
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE The M235T mutation of the human angiotensinogen gene has been shown to be associated with elevated circulating angiotensinogen concentrations and essential hypertension. 16940224 2006
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE Strong epistatic interactions were found between -6G>A, M235T and -217G>A markers, supporting the synergistic effect between them leading to EHT. 22570327 2012
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE Thus, if the Met235-->Thr variant of AGT is involved in essential HT, then its contribution may be, at best, much weaker in other HT groups. 8267622 1993
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE In the present study we examined the genotype frequencies of the insertion/deletion polymorphisms of the ACE gene and the M235T polymorphism of the Angiotensinogen (Agt) gene in patients with essential hypertension in comparison with normotensive subjects. 9524045 1998
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE We studied the effects of the angiotensinogen M235T, angiotensin converting enzyme insertion/deletion (ACE I/D), and angiotensin II receptor 1 (AT1R) A1166C gene polymorphisms on the risk of HTA and to evaluate the relationship between these polymorphisms and obesity. 21779803 2012
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE According to combined haplotype analysis of diallele and microsatellite markers, it remains a possibility that M235T, T+31C, G-6A, A-20C and G-1074T polymorphisms may play an important role in increased risk for essential hypertension. 11191642 2000
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE The results of our study suggest an association of the M235T polymorphism in the gene encoding angiotensinogen with essential hypertension. 12169209 2003
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE The TT genotype of a polymorphism encoding threonine instead of methionine (M235T) has been associated not only with increased plasma angiotensinogen concentration but also with essential hypertension. 8593944 1996
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
0.100 GeneticVariation BEFREE We determined the association of angiotensinogen (M235T) gene polymorphism with essential hypertension and the relationship between polymorphism in the angiotensinogen (M235T) gene and blood pressure response to ACE inhibitor (Enalapril) in patients with essential hypertension from northern Indian subjects. 22974788 2012