rs779188587
|
|
Allanson Pantzar McLeod syndrome
|
C |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs778390161
|
|
Allanson Pantzar McLeod syndrome
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs397514689
|
|
Allanson Pantzar McLeod syndrome
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs397514688
|
|
Allanson Pantzar McLeod syndrome
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs387906576
|
|
Allanson Pantzar McLeod syndrome
|
C |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912704
|
|
Allanson Pantzar McLeod syndrome
|
G |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs121912703
|
|
ANGIOTENSIN I-CONVERTING ENZYME, BENIGN SERUM INCREASE
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs1267969615
|
|
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 |
rs1267969615
|
|
Myocardial Infarction
|
|
0.100 |
GeneticVariation
|
BEFREE |
The angiotensinogen-TT genotype (T indicates threonine instead of methionine at position 235) was more frequent in the myocardial infarction group than in the control group (P < .05).
|
7737732 |
1995 |
rs371010069
|
|
Hypertrophic Cardiomyopathy
|
|
0.010 |
GeneticVariation
|
BEFREE |
Several mutations such as Arg403Gln and Arg719Gln are associated with a high incidence of SCD, while Leu908Val mutation is associated with a benign course and a low incidence of SCD in HCM families.
|
7788945 |
1995 |
rs1267969615
|
|
Retinal Diseases
|
|
0.010 |
GeneticVariation
|
BEFREE |
Association with the I/D polymorphism of the ACE gene and M235T variant of the angiotensinogen gene (AGT) with microalbuminuria and retinopathy was examined.
|
8587251 |
1995 |
rs1267969615
|
|
Diabetic Nephropathy
|
|
0.100 |
GeneticVariation
|
BEFREE |
These results suggested that ACE I/D polymorphism, but not AGN M235T polymorphism, is a possible genetic risk factor for diabetic nephropathy in Japanese NIDDM patients.
|
8596493 |
1996 |
rs1267969615
|
|
Diabetic Nephropathy
|
|
0.100 |
GeneticVariation
|
BEFREE |
We have examined the angiotensin converting enzyme insertion/deletion polymorphism and angiotensinogen methionine 235 threonine polymorphism in a large cohort of Caucasian patients with IDDM and diabetic nephropathy.
|
8877296 |
1996 |
rs1267969615
|
|
Myocardial Infarction
|
|
0.100 |
GeneticVariation
|
BEFREE |
The purpose of the present study was to assess whether the insertion (I)/deletion (D) polymorphism of the angiotensin converting enzyme (ACE) gene, and the polymorphism of angiotensinogen (AGT) gene with threonine (T) instead of methionine (M) at amino acid 235 in exon 2 (M235T) were associated with left ventricular dilatation after myocardial infarction.
|
8793580 |
1996 |
rs1267969615
|
|
Diabetes Mellitus, Insulin-Dependent
|
|
0.040 |
GeneticVariation
|
BEFREE |
We have examined the angiotensin converting enzyme insertion/deletion polymorphism and angiotensinogen methionine 235 threonine polymorphism in a large cohort of Caucasian patients with IDDM and diabetic nephropathy.
|
8877296 |
1996 |
rs1267969615
|
|
Left ventricular dilatation
|
|
0.010 |
GeneticVariation
|
BEFREE |
The purpose of the present study was to assess whether the insertion (I)/deletion (D) polymorphism of the angiotensin converting enzyme (ACE) gene, and the polymorphism of angiotensinogen (AGT) gene with threonine (T) instead of methionine (M) at amino acid 235 in exon 2 (M235T) were associated with left ventricular dilatation after myocardial infarction.
|
8793580 |
1996 |
rs1267969615
|
|
Hypertensive disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
In studies conducted in several different populations, the M235T substitution in the angiotensinogen (AGT) locus has been associated with hypertension.
|
9034402 |
1997 |
rs1267969615
|
|
Myocardial Infarction
|
|
0.100 |
GeneticVariation
|
BEFREE |
This case-control study was initiated to investigate whether the ACEI/D and AGT M235T polymorphisms are associated with an increased risk for coronary heart disease (CHD) and MI.
|
9034401 |
1997 |
rs1267969615
|
|
Hypertensive disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
Furthermore, an M235T variant of the angiotensinogen (AGT) gene has been associated with hypertension, an important risk factor for the development and progression of diabetic nephropathy.
|
9049480 |
1997 |
rs1267969615
|
|
Essential Hypertension
|
|
0.100 |
GeneticVariation
|
BEFREE |
To examine whether the angiotensinogen M235T and angiotensin converting enzyme insertion/deletion (I/D) variants are related to the severity of hypertension in patients with established essential hypertension.
|
9170002 |
1997 |
rs1267969615
|
|
Diabetic Nephropathy
|
|
0.100 |
GeneticVariation
|
BEFREE |
Furthermore, an M235T variant of the angiotensinogen (AGT) gene has been associated with hypertension, an important risk factor for the development and progression of diabetic nephropathy.
|
9049480 |
1997 |
rs1267969615
|
|
Hypertensive disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
To examine whether the angiotensinogen M235T and angiotensin converting enzyme insertion/deletion (I/D) variants are related to the severity of hypertension in patients with established essential hypertension.
|
9170002 |
1997 |
rs1267969615
|
|
Coronary heart disease
|
|
0.080 |
GeneticVariation
|
BEFREE |
This case-control study was initiated to investigate whether the ACEI/D and AGT M235T polymorphisms are associated with an increased risk for coronary heart disease (CHD) and MI.
|
9034401 |
1997 |
rs1267969615
|
|
Coronary heart disease
|
|
0.080 |
GeneticVariation
|
BEFREE |
We found a correlation between the M235T molecular variant of AGT and the S128R variant of E-selectin to early severe CHD.
|
9020385 |
1997 |
rs1267969615
|
|
IGA Glomerulonephritis
|
|
0.070 |
GeneticVariation
|
BEFREE |
We examined whether the M235T polymorphism of the angiotensinogen (AGT) gene, the insertion/deletion polymorphism of the angiotensin-converting enzyme (ACE) gene, and the A1166--> C polymorphism of the angiotensin II type 1 receptor gene may be associated with disease progression in 168 Caucasian patients with IgA nephropathy.
|
9259580 |
1997 |