Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma. 27539324

2016

dbSNP: rs587782604
rs587782604
A 0.700 CausalMutation CLINVAR Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma. 27539324

2016

dbSNP: rs587782604
rs587782604
A 0.700 CausalMutation CLINVAR SDHD immunohistochemistry: a new tool to validate SDHx mutations in pheochromocytoma/paraganglioma. 25405498

2015

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice. 25695889

2015

dbSNP: rs587782604
rs587782604
A 0.700 CausalMutation CLINVAR Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum. 26259135

2015

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum. 26259135

2015

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR [Intrapericardical paraganglioma associated with mutation in succinate dehydrogenase enzyme gene]. 24939699

2015

dbSNP: rs587782604
rs587782604
A 0.700 CausalMutation CLINVAR Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families. 23934599

2014

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR SDHB gene mutation in a carotid body paraganglioma: case report and review of the paraganglioma syndromes. 24509376

2014

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer. 23083876

2012

dbSNP: rs587782604
rs587782604
A 0.700 CausalMutation CLINVAR Mutation of SDHB is a cause of hypoxia-related high-altitude paraganglioma. 20592014

2010

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Mutation of SDHB is a cause of hypoxia-related high-altitude paraganglioma. 20592014

2010

dbSNP: rs587782604
rs587782604
A 0.700 CausalMutation CLINVAR Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out. 19351833

2009

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out. 19351833

2009

dbSNP: rs587782604
rs587782604
A 0.700 CausalMutation CLINVAR Germline SDHB mutations are common in patients with apparently sporadic sympathetic paragangliomas. 18382370

2008

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Hereditary paraganglioma of the nasopharynx. 20614293

2008

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Germline SDHB mutations are common in patients with apparently sporadic sympathetic paragangliomas. 18382370

2008

dbSNP: rs587782604
rs587782604
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: rs587782604
rs587782604
A 0.700 CausalMutation CLINVAR High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing. 16912137

2006

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Genetic testing in pheochromocytoma or functional paraganglioma. 16314641

2005

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. 14500403

2003