Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315366
rs74315366
SDHB
A 0.700 CausalMutation CLINVAR SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations. 28374168

2017
dbSNP: rs74315366
rs74315366
SDHB
A 0.700 CausalMutation CLINVAR Calculating the optimal surveillance for head and neck paraganglioma in SDHB-mutation carriers. 27573198

2017
dbSNP: rs74315366
rs74315366
SDHB
A 0.700 CausalMutation CLINVAR A Duodenal SDH-Deficient Gastrointestinal Stromal Tumor in a Patient With a Germline SDHB Mutation. 28324028

2017
dbSNP: rs74315366
rs74315366
SDHB
A 0.700 CausalMutation CLINVAR Attention Deficit Hyperactivity Disorder in Pediatric Patients with Pheochromocytoma and Paraganglioma. 27171833

2016
dbSNP: rs74315366
rs74315366
SDHB
A 0.700 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2015
dbSNP: rs74315366
rs74315366
SDHB
A 0.700 CausalMutation CLINVAR Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer. 23083876

2012
dbSNP: rs74315366
rs74315366
SDHB
A 0.700 CausalMutation CLINVAR Renal tumors associated with germline SDHB mutation show distinctive morphology. 21934479

2011
dbSNP: rs74315366
rs74315366
SDHB
A 0.700 CausalMutation CLINVAR Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. 16317055

2006
dbSNP: rs74315366
rs74315366
SDHB
A 0.700 CausalMutation CLINVAR Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. 11404820

2001