rs727503166
|
|
Cardiomyopathy, Hypertrophic, Familial
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.
|
20031619 |
2009 |
rs727503166
|
|
Cardiomyopathy, Hypertrophic, Familial
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
rs727503166
|
|
Cardiomyopathy, Hypertrophic, Familial
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Expression patterns of cardiac myofilament proteins: genomic and protein analysis of surgical myectomy tissue from patients with obstructive hypertrophic cardiomyopathy.
|
19808356 |
2009 |
rs727503166
|
|
Cardiomyopathy, Hypertrophic, Familial
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy.
|
18533079 |
2008 |
rs727503166
|
|
Cardiomyopathy, Hypertrophic, Familial
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing.
|
23396983 |
2013 |
rs727503166
|
|
Cardiomyopathy, Hypertrophic, Familial
|
C |
0.700 |
CausalMutation
|
CLINVAR |
The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening.
|
20019025 |
2010 |
rs727503166
|
|
Cardiomyopathy, Hypertrophic, Familial
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.
|
25611685 |
2015 |
rs727503166
|
|
Cardiomyopathy, Hypertrophic, Familial
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Hypertrophic cardiomyopathy clinical phenotype is independent of gene mutation and mutation dosage.
|
29121657 |
2017 |
rs727503166
|
|
Cardiomyopathy, Hypertrophic, Familial
|
C |
0.700 |
CausalMutation
|
CLINVAR |
Mortality risk of untreated myosin-binding protein C-related hypertrophic cardiomyopathy: insight into the natural history.
|
22115648 |
2011 |