|
rs1799983
|
|
|
0.060 |
GeneticVariation |
BEFREE |
Heart failure and endothelial nitric oxide synthase G894T gene polymorphism frequency variations within ancestries.
|
28554876 |
2018 |
|
rs1042713
|
|
|
0.040 |
GeneticVariation |
BEFREE |
Arginine 16 glycine beta2-adrenoceptor polymorphism and cardiovascular structure and function in patients with heart failure.
|
17336757 |
2007 |
|
rs1320702652
|
|
|
0.040 |
GeneticVariation |
BEFREE |
C34T AMPD1 polymorphism may be associated with reduced frequency of obesity in CAD patients and of hyperglycaemia and diabetes in both CAD and HF patients.
|
18855224 |
2009 |
|
rs121918080
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A 47-year-old man started developing severe diarrhea and weight loss at age 41 years, followed by urinary incontinence, autonomic-nervous-system abnormalities and serious heart failure; the diagnosis of FAP (ATTR Ser50Ile) was made on the basis of genetic, histochemical and immunohistochemical analysis.
|
10834537 |
2000 |
|
rs10927887
|
|
|
0.020 |
GeneticVariation |
BEFREE |
A CLCNKA polymorphism (rs10927887; p.Arg83Gly) previously linked to heart failure is associated with the estimated glomerular filtration rate in the RENASTUR cohort.
|
23850580 |
2013 |
|
rs1800730
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A rare S65C mutation and a novel A271S mutation were also found in this study; the latter patient had 4+ iron in the liver and later developed heart failure with cardiac iron.
|
20208481 |
2010 |
|
rs1337916669
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A rare S65C mutation and a novel A271S mutation were also found in this study; the latter patient had 4+ iron in the liver and later developed heart failure with cardiac iron.
|
20208481 |
2010 |
|
rs762151808
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A rare S65C mutation and a novel A271S mutation were also found in this study; the latter patient had 4+ iron in the liver and later developed heart failure with cardiac iron.
|
20208481 |
2010 |
|
rs9909004
|
|
|
0.020 |
GeneticVariation |
BEFREE |
A recently discovered cardiac-specific regulatory variant for PRKCA (rs9909004) was independently associated with a decreased risk for all-cause mortality in patients with HF.
|
31728800 |
2019 |
|
rs397516089
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A second pediatric patient presented with heart failure and was found to carry a de novo MYH7 R369Q mutation.
|
20031619 |
2009 |
|
rs5443
|
|
|
0.020 |
GeneticVariation |
BEFREE |
A total of 350 subjects enrolled in the genetic substudy (GRAHF [Genetic Risk Assessment of Heart Failure in African Americans]) were genotyped for the C825T polymorphism.
|
25306451 |
2014 |
|
rs1429117513
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A total of 350 subjects enrolled in the genetic substudy (GRAHF [Genetic Risk Assessment of Heart Failure in African Americans]) were genotyped for the C825T polymorphism.
|
25306451 |
2014 |
|
rs1042713
|
|
|
0.040 |
GeneticVariation |
BEFREE |
ADRB2 polymorphism Arg16Gly modifies the natural outcome of heart failure and dictates therapeutic response to β-blockers in patients with heart failure.
|
30374408 |
2018 |
|
rs1258130495
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ADRB2 polymorphism Arg16Gly modifies the natural outcome of heart failure and dictates therapeutic response to β-blockers in patients with heart failure.
|
30374408 |
2018 |
|
rs671
|
|
|
0.020 |
GeneticVariation |
BEFREE |
ALDH2 rs671 polymorphism is proven to be closely related to the prevalence of CAD, hypertension, diabetes mellitus and alcoholism, which are etiological factors of heart failure.
|
27742538 |
2017 |
|
rs10501920
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Also, rs10501920 in CNTN5 was associated with AF (p = 9.4 x 10(-6)) and HF (p = 1.2 x 10(-4)).
|
17903304 |
2007 |
|
rs2149954
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Altogether, nominally significant associations between the rs2149954 minor allele and a decreased risk of heart attack and heart failure as well as increased physical functioning were found in the long-lived individuals.
|
28100865 |
2017 |
|
rs76992529
|
|
|
0.060 |
GeneticVariation |
BEFREE |
Among individuals of African or Hispanic/Latino ancestry enrolled in 2 academic medical center-based biobanks, the TTR V122I genetic variant was significantly associated with heart failure.
|
31821430 |
2019 |
|
rs1801253
|
|
|
0.100 |
GeneticVariation |
BEFREE |
An evaluation of the beta-1 adrenergic receptor Arg389Gly polymorphism in individuals with heart failure: a MERIT-HF sub-study.
|
12921807 |
2003 |
|
rs699
|
|
|
0.040 |
GeneticVariation |
BEFREE |
Angiotensinogen M235T and T174M gene polymorphisms in combination doubles the risk of mortality in heart failure.
|
17145981 |
2007 |
|
rs10519210
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
|
20445134 |
2010 |
|
rs10519210
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
|
20445134 |
2010 |
|
rs11172782
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
|
20445134 |
2010 |
|
rs11172782
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
|
20445134 |
2010 |
|
rs1520832
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
|
20445134 |
2010 |