rs12720459
|
|
|
0.850 |
GeneticVariation |
UNIPROT |
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
|
27854360 |
2017 |
rs12720459
|
|
|
0.850 |
GeneticVariation |
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
rs12720459
|
|
|
0.850 |
GeneticVariation |
UNIPROT |
Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.
|
23994779 |
2013 |
rs12720459
|
|
|
0.850 |
GeneticVariation |
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
rs12720459
|
|
|
0.850 |
GeneticVariation |
UNIPROT |
HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).
|
21810866 |
2011 |
rs120074191
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
|
27854360 |
2017 |
rs120074193
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
|
27854360 |
2017 |
rs199472755
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
|
27854360 |
2017 |
rs120074178
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndrome.
|
25705178 |
2015 |
rs120074191
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndrome.
|
25705178 |
2015 |
rs120074191
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
rs120074193
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndrome.
|
25705178 |
2015 |
rs120074193
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
rs199472755
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
rs199472755
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndrome.
|
25705178 |
2015 |
rs199472804
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndrome.
|
25705178 |
2015 |
rs199473457
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndrome.
|
25705178 |
2015 |
rs120074178
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A molecular mechanism for adrenergic-induced long QT syndrome.
|
24184248 |
2014 |
rs120074191
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A molecular mechanism for adrenergic-induced long QT syndrome.
|
24184248 |
2014 |
rs120074193
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A molecular mechanism for adrenergic-induced long QT syndrome.
|
24184248 |
2014 |
rs199472755
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A molecular mechanism for adrenergic-induced long QT syndrome.
|
24184248 |
2014 |
rs199472804
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A molecular mechanism for adrenergic-induced long QT syndrome.
|
24184248 |
2014 |
rs199473457
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A molecular mechanism for adrenergic-induced long QT syndrome.
|
24184248 |
2014 |
rs120074178
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.
|
23994779 |
2013 |
rs120074191
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |