|
rs5186
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Among individuals with essential hypertension certain relationships were documented between rs5182 and rs5186 polymorphisms of AGTR1 gene and rs1799998 polymorphism of CYP11B2 gene on one hand and the volume of carotid bodies on one other.
|
29627490 |
2018 |
|
rs5186
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Essential hypertension patients were genotyped for 11 polymorphisms of essential hypertension susceptibility genes including ADD1 (rs4961), GNB3 (rs5443, rs16932941), NOS3 (rs1799983, rs2070744), ACE (rs5186), AGTR1 (rs5186), AGT (rs699, rs4762), MR (rs5534), and TGFB1 (rs1800471).
|
26335431 |
2015 |
|
rs5186
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The present study is about a particular genetic polymorphism (A1166C), gene expression and protein expression of the angiotensin II type I receptor (AT1R) (SNP ID: rs5186) and its association with essential hypertension in a Northern Indian population.
|
24992666 |
2014 |
|
rs5182
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Among individuals with essential hypertension certain relationships were documented between rs5182 and rs5186 polymorphisms of AGTR1 gene and rs1799998 polymorphism of CYP11B2 gene on one hand and the volume of carotid bodies on one other.
|
29627490 |
2018 |
|
rs5182
|
|
|
0.020 |
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 |
|
rs2638360
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Meta-analysis revealed that C allele of rs2638360 could significantly increase the risk of essential hypertension.
|
25628312 |
2015 |
|
rs387967
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our findings suggest that rs387967 is associated with the susceptibility to essential hypertension in a Yi population and the tendency was replicated in systolic blood pressure and diastolic blood pressure detection.
|
25628312 |
2015 |
|
rs12695895
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The present results indicate that rs12695895 might be a genetic marker for EH and Hap4 (AGGACTT) was associated with hypertension in Han Chinese population.
|
19833117 |
2010 |
|
rs911154679
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Constitutively activated GRK4 gene variants (R65L, A142V, and A486V), by themselves or by their interaction with other genes involved in blood pressure regulation, are associated with essential hypertension and/or salt-sensitive hypertension in several ethnic groups.
|
20153824 |
2010 |
|
rs777986489
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Both newly detected TSC C1784T and ADRB3 T727C are gene polymorphisms susceptible to the antihypertensive effect of TZDs in patients with EHT.
|
15824464 |
2004 |