rs121913647
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555338080
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs377491278
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs397516089
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
rs397516122
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs397516123
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs397516142
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
rs397516142
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathy.
|
21211974 |
2011 |
rs397516165
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians.
|
25448463 |
2014 |
rs397516165
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.
|
21750094 |
2011 |
rs397516165
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Loss of Function Mutations in NNT Are Associated With Left Ventricular Noncompaction.
|
26025024 |
2015 |
rs397516165
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
rs397516165
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Electrocardiographic features of sarcomere mutation carriers with and without clinically overt hypertrophic cardiomyopathy.
|
21943931 |
2011 |
rs397516224
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs397516248
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
165th ENMC International Workshop: distal myopathies 6-8th February 2009 Naarden, The Netherlands.
|
19477645 |
2009 |
rs397516252
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs397516253
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs397516254
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
rs397516254
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy.
|
24664454 |
2014 |
rs397516258
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene.
|
15769782 |
2005 |
rs45516091
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs45544633
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Prognostic Relevance of Gene-Environment Interactions in Patients With Dilated Cardiomyopathy: Applying the MOGE(S) Classification.
|
26383716 |
2015 |
rs45544633
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.
|
22337857 |
2012 |
rs45544633
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
A de novo germline mutation in MYH7 causes a progressive dominant myopathy in pigs.
|
23153285 |
2012 |
rs45544633
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
|
24119082 |
2013 |