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 | Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort. | 25494863 | 2015 |
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T | 0.700 | CausalMutation | CLINVAR | Genetic testing in head and neck paraganglioma: who, what, and why? | 24436918 | 2013 |
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T | 0.700 | CausalMutation | CLINVAR | Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations. | 23433498 | 2013 |
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T | 0.700 | CausalMutation | CLINVAR | High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands. | 21348866 | 2012 |
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T | 0.700 | CausalMutation | CLINVAR | Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect. | 21937622 | 2011 |
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T | 0.700 | CausalMutation | CLINVAR | The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. | 19454582 | 2009 |
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T | 0.700 | CausalMutation | CLINVAR | SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas. | 15479192 | 2004 |
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T | 0.700 | CausalMutation | CLINVAR | Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. | 11897817 | 2002 |
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T | 0.700 | CausalMutation | CLINVAR | Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss. | 11391796 | 2001 |
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T | 0.700 | CausalMutation | CLINVAR | Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. | 10657297 | 2000 |