|
rs1344172059
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs141322087
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs1553265736
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs1559279177
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs587782927
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs748379243
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs766265889
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs794728602
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs8259
|
|
|
0.010 |
GeneticVariation |
BEFREE |
<i>BSG</i> rs8259 polymorphism may contribute to decreased risk of CHF in a Chinese Han population.
|
28230811 |
2017 |
|
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 |
|
rs1815739
|
|
|
0.010 |
GeneticVariation |
BEFREE |
R577X polymorphism in the ACTN3 gene was independently associated with worse survival in patients with chronic heart failure.
|
25059829 |
2014 |
|
rs28714259
|
|
|
0.010 |
GeneticVariation |
BEFREE |
rs28714259 represents a validated SNP that is associated with anthracycline-induced CHF in three independent, phase III adjuvant breast cancer clinical trials.
|
27993963 |
2017 |
|
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 |
|
rs767312316
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A stop‑gain mutation in urotensin II receptor (UTS2R) (p.S241X), which is associated with congestive heart failure, was identified in the proband and in one other affected family member.
|
25997934 |
2015 |
|
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 |
|
rs76992529
|
|
|
0.070 |
GeneticVariation |
BEFREE |
After the age of 65 years (CHS), the frequencies of congestive heart failure (38% vs 15%, relative risk 2.62, P = .04) and mortality (76% vs 53%, relative risk 1.46, P = .08) were higher in V122I allele carriers than in age-, gender- and ethnically matched controls.
|
20435197 |
2010 |