| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
0.800 | GeneticVariation | UNIPROT | American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers. | 24493721 | 2014 |
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|
0.800 | GeneticVariation | UNIPROT | Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. | 24893135 | 2014 |
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|
0.800 | GeneticVariation | UNIPROT | Canadian guideline on genetic screening for hereditary renal cell cancers. | 24319509 | 2013 |
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|
0.800 | GeneticVariation | UNIPROT | Somatic SDHB mutation in an extraadrenal pheochromocytoma. | 17634472 | 2007 |
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|
0.800 | GeneticVariation | UNIPROT | Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. | 15328326 | 2004 |
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|
0.800 | GeneticVariation | UNIPROT | Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility. | 14974914 | 2003 |
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|
0.800 | GeneticVariation | UNIPROT | Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. | 14500403 | 2003 |
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|
0.800 | GeneticVariation | UNIPROT | 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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|
0.800 | GeneticVariation | UNIPROT | Germ-line mutations in nonsyndromic pheochromocytoma. | 12000816 | 2002 |
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|
0.800 | GeneticVariation | UNIPROT | Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. | 11404820 | 2001 |
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|
T | 0.800 | CausalMutation | CLINVAR |