rs74315380
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
A |
0.800 |
CausalMutation
|
CLINVAR |
Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
|
24119082 |
2013 |
rs74315380
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
A |
0.800 |
CausalMutation
|
CLINVAR |
Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates.
|
22675533 |
2012 |
rs74315380
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
A |
0.800 |
CausalMutation
|
CLINVAR |
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
|
21551322 |
2011 |
rs74315380
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
A |
0.800 |
CausalMutation
|
CLINVAR |
Mutations in sarcomere protein genes in left ventricular noncompaction.
|
18506004 |
2008 |
rs74315380
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
A |
0.800 |
CausalMutation
|
CLINVAR |
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
|
17932326 |
2007 |
rs74315380
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
A |
0.800 |
CausalMutation
|
CLINVAR |
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
|
15923195 |
2005 |
rs74315380
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
A |
0.800 |
CausalMutation
|
CLINVAR |
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
|
15542288 |
2004 |
rs74315380
|
|
Cardiomyopathy, Dilated
|
A |
0.720 |
GeneticVariation
|
CLINVAR |
Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates.
|
22675533 |
2012 |
rs74315380
|
|
Cardiomyopathy, Dilated
|
A |
0.720 |
GeneticVariation
|
CLINVAR |
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
|
21551322 |
2011 |
rs74315380
|
|
Cardiomyopathy, Dilated
|
A |
0.720 |
GeneticVariation
|
CLINVAR |
Mutations in sarcomere protein genes in left ventricular noncompaction.
|
18506004 |
2008 |
rs74315380
|
|
Cardiomyopathy, Dilated
|
A |
0.720 |
GeneticVariation
|
CLINVAR |
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
|
17932326 |
2007 |
rs74315380
|
|
Cardiomyopathy, Dilated
|
A |
0.720 |
GeneticVariation
|
CLINVAR |
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
|
15923195 |
2005 |
rs74315380
|
|
Cardiomyopathy, Dilated
|
A |
0.720 |
GeneticVariation
|
CLINVAR |
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
|
15542288 |
2004 |
rs74315380
|
|
Cardiomyopathy, Familial Hypertrophic, 2
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
|
24119082 |
2013 |
rs74315380
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
|
24119082 |
2013 |
rs74315380
|
|
Cardiomyopathy, Familial Hypertrophic, 2
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates.
|
22675533 |
2012 |
rs74315380
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates.
|
22675533 |
2012 |
rs74315380
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
|
21551322 |
2011 |
rs74315380
|
|
Cardiomyopathy, Familial Hypertrophic, 2
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
|
21551322 |
2011 |
rs74315380
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Mutations in sarcomere protein genes in left ventricular noncompaction.
|
18506004 |
2008 |
rs74315380
|
|
Cardiomyopathy, Familial Hypertrophic, 2
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Mutations in sarcomere protein genes in left ventricular noncompaction.
|
18506004 |
2008 |
rs74315380
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
|
17932326 |
2007 |
rs74315380
|
|
Cardiomyopathy, Familial Hypertrophic, 2
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
|
17932326 |
2007 |
rs74315380
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
|
15923195 |
2005 |
rs74315380
|
|
Cardiomyopathy, Familial Hypertrophic, 2
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
|
15923195 |
2005 |