Variant Gene Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607032
rs267607032
0.700 GeneticVariation CLINVAR The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers. 28503760

2018

dbSNP: rs772551056
rs772551056
0.700 CausalMutation CLINVAR The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers. 28503760

2018

dbSNP: rs267607032
rs267607032
0.700 GeneticVariation CLINVAR The phenotype of SDHB germline mutation carriers: a nationwide study. 28490599

2017

dbSNP: rs267607032
rs267607032
0.700 GeneticVariation CLINVAR SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations. 28374168

2017

dbSNP: rs74315366
rs74315366
0.700 CausalMutation CLINVAR Attention Deficit Hyperactivity Disorder in Pediatric Patients with Pheochromocytoma and Paraganglioma. 27171833

2017

dbSNP: rs74315366
rs74315366
0.700 CausalMutation CLINVAR Calculating the optimal surveillance for head and neck paraganglioma in SDHB-mutation carriers. 27573198

2017

dbSNP: rs772551056
rs772551056
0.700 CausalMutation CLINVAR A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGL. 27700540

2017

dbSNP: rs772551056
rs772551056
0.700 CausalMutation CLINVAR The phenotype of SDHB germline mutation carriers: a nationwide study. 28490599

2017

dbSNP: rs772551056
rs772551056
0.700 CausalMutation CLINVAR SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations. 28374168

2017

dbSNP: rs397516833
rs397516833
0.700 CausalMutation CLINVAR Pyruvate carboxylation enables growth of SDH-deficient cells by supporting aspartate biosynthesis. 26302408

2016

dbSNP: rs397516836
rs397516836
0.700 CausalMutation CLINVAR Carney triad can be (rarely) associated with germline succinate dehydrogenase defects. 26173966

2016

dbSNP: rs398122805
rs398122805
0.700 CausalMutation CLINVAR Sporadic paraganglioma caused by de novo SDHB mutations in a 6-year-old girl. 26283294

2016

dbSNP: rs587782604
rs587782604
0.700 GeneticVariation CLINVAR Usefulness of Somatostatin Receptor Scintigraphy (Tc-[HYNIC, Tyr3]-Octreotide) and 123I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed Tomography. 25791839

2016

dbSNP: rs74315366
rs74315366
0.700 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2016

dbSNP: rs74315367
rs74315367
0.700 GeneticVariation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2016

dbSNP: rs74315368
rs74315368
0.700 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2016

dbSNP: rs74315368
rs74315368
0.700 CausalMutation CLINVAR Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy. 25736212

2016

dbSNP: rs74315368
rs74315368
0.700 CausalMutation CLINVAR Superiority of [68Ga]-DOTATATE PET/CT to Other Functional Imaging Modalities in the Localization of SDHB-Associated Metastatic Pheochromocytoma and Paraganglioma. 25873086

2016

dbSNP: rs74315369
rs74315369
0.700 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2016

dbSNP: rs74315370
rs74315370
0.700 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2016

dbSNP: rs74315370
rs74315370
0.700 CausalMutation CLINVAR 15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5. 26273102

2016

dbSNP: rs747198089
rs747198089
0.700 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2016

dbSNP: rs772551056
rs772551056
0.700 CausalMutation CLINVAR SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery. 26719882

2016

dbSNP: rs772551056
rs772551056
0.700 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2016

dbSNP: rs786201095
rs786201095
0.700 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2016