rs397516471
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
|
28669108 |
2017 |
rs397516471
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Multiple Species Comparison of Cardiac Troponin T and Dystrophin: Unravelling the DNA behind Dilated Cardiomyopathy.
|
29367539 |
2017 |
rs397516471
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosin.
|
24367593 |
2013 |
rs397516471
|
|
Cardiomyopathy, Familial Hypertrophic, 2
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathy.
|
24205113 |
2013 |
rs397516471
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathy.
|
24205113 |
2013 |
rs397516471
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosin.
|
24367593 |
2013 |
rs397516471
|
|
Cardiomyopathy, Familial Hypertrophic, 2
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosin.
|
24367593 |
2013 |
rs397516471
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathy.
|
24205113 |
2013 |
rs397516471
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Genetic testing for dilated cardiomyopathy in clinical practice.
|
22464770 |
2012 |
rs397516471
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.
|
21310275 |
2011 |
rs397516471
|
|
Cardiomyopathy, Familial Hypertrophic, 2
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.
|
21310275 |
2011 |
rs397516471
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.
|
21310275 |
2011 |
rs397516471
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Dilated cardiomyopathy caused by a novel TNNT2 mutation-added value of genetic testing in the correct identification of affected subjects.
|
19324435 |
2010 |
rs397516471
|
|
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Dilated cardiomyopathy caused by a novel TNNT2 mutation-added value of genetic testing in the correct identification of affected subjects.
|
19324435 |
2010 |
rs397516471
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Dilated cardiomyopathy caused by a novel TNNT2 mutation-added value of genetic testing in the correct identification of affected subjects.
|
19324435 |
2010 |
rs397516471
|
|
Cardiomyopathy, Familial Hypertrophic, 2
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Dilated cardiomyopathy caused by a novel TNNT2 mutation-added value of genetic testing in the correct identification of affected subjects.
|
19324435 |
2010 |