Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies. 24781345

2014

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma. 23666964

2013

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function. 22835832

2012

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Bilateral adrenal medullary hyperplasia associated with an SDHB mutation. 21172883

2011

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582

2009

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Biochemically silent abdominal paragangliomas in patients with mutations in the succinate dehydrogenase subunit B gene. 18840642

2008

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Clinical presentations, biochemical phenotypes, and genotype-phenotype correlations in patients with succinate dehydrogenase subunit B-associated pheochromocytomas and paragangliomas. 17200167

2007

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas. 17652212

2007

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. 16317055

2006

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing. 16912137

2006

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Genetic testing in pheochromocytoma or functional paraganglioma. 16314641

2005

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. 15328326

2004

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Germ-line mutations in nonsyndromic pheochromocytoma. 12000816

2002