|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Malignant effects of multiple rare variants in sarcomere genes on the prognosis of patients with hypertrophic cardiomyopathy.
|
25132132 |
2014 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants.
|
23299917 |
2013 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells.
|
23290139 |
2013 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy.
|
23283745 |
2013 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Haplotype sharing test maps genes for familial cardiomyopathies.
|
20573160 |
2011 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation.
|
10750581 |
1999 |
|
| Entrez Id: |
4625 |
| Gene Symbol: |
MYH7 |
MYH7
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
4000 |
| Gene Symbol: |
LMNA |
LMNA
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
1674 |
| Gene Symbol: |
DES |
DES
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
282996 |
| Gene Symbol: |
RBM20 |
RBM20
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
4633 |
| Gene Symbol: |
MYL2 |
MYL2
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
282996 |
| Gene Symbol: |
RBM20 |
RBM20
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
4000 |
| Gene Symbol: |
LMNA |
LMNA
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
7273 |
| Gene Symbol: |
TTN |
TTN
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
5318 |
| Gene Symbol: |
PKP2 |
PKP2
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
91624 |
| Gene Symbol: |
NEXN |
NEXN
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
100506866 |
| Gene Symbol: |
TTN-AS1 |
TTN-AS1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
1674 |
| Gene Symbol: |
DES |
DES
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|