Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
A | 0.700 | CausalMutation | CLINVAR | Clinical exome sequencing for genetic identification of rare Mendelian disorders. | 25326637 | 2014 |
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|
A | 0.700 | CausalMutation | CLINVAR | Integrative genetic characterization and phenotype correlations in pheochromocytoma and paraganglioma tumours. | 24466223 | 2014 |
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|
A | 0.700 | CausalMutation | CLINVAR | Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer. | 23083876 | 2012 |
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|
A | 0.700 | CausalMutation | CLINVAR | High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands. | 21348866 | 2012 |
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|
A | 0.700 | CausalMutation | CLINVAR | Renal tumors associated with germline SDHB mutation show distinctive morphology. | 21934479 | 2011 |
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|
A | 0.700 | CausalMutation | CLINVAR | The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. | 19454582 | 2009 |
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|
A | 0.700 | CausalMutation | CLINVAR | Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B (SDH-B) gene mutation carriers. | 18419787 | 2008 |
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|
A | 0.700 | CausalMutation | CLINVAR | Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. | 16317055 | 2006 |
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|
A | 0.700 | CausalMutation | CLINVAR | Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. | 12618761 | 2003 |
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|
A | 0.700 | CausalMutation | CLINVAR | Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. | 11404820 | 2001 |