Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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T | 0.700 | CausalMutation | CLINVAR | Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan. | 18646565 | 2007 |
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T | 0.700 | CausalMutation | CLINVAR | Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation. | 15053843 | 2004 |
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T | 0.700 | CausalMutation | CLINVAR | Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype. | 12673789 | 2003 |
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T | 0.700 | CausalMutation | CLINVAR | Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers. | 23183350 | 2013 |
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T | 0.700 | CausalMutation | CLINVAR | Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers. | 16386954 | 2006 |
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T | 0.700 | CausalMutation | CLINVAR | Inflammatory changes in infantile-onset LMNA-associated myopathy. | 21632249 | 2011 |
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T | 0.700 | CausalMutation | CLINVAR | MicroRNA expression profiling in patients with lamin A/C-associated muscular dystrophy. | 21840938 | 2011 |
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T | 0.700 | CausalMutation | CLINVAR | Natural history of dilated cardiomyopathy due to lamin A/C gene mutations. | 12628721 | 2003 |
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T | 0.700 | CausalMutation | CLINVAR | The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing. | 24503780 | 2014 |