Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315367
rs74315367
SDHB
C 0.800 GeneticVariation CLINVAR

dbSNP: rs74315367
rs74315367
SDHB
C 0.800 CausalMutation CLINVAR

dbSNP: rs74315368
rs74315368
SDHB
T 0.800 CausalMutation CLINVAR Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy. 25736212

2015
dbSNP: rs74315368
rs74315368
SDHB
T 0.800 CausalMutation CLINVAR Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management. 20208144

2010
dbSNP: rs74315368
rs74315368
SDHB
T 0.800 CausalMutation CLINVAR Germ-line mutations in nonsyndromic pheochromocytoma. 12000816

2002
dbSNP: rs74315368
rs74315368
SDHB
T 0.800 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2015
dbSNP: rs74315368
rs74315368
SDHB
T 0.800 CausalMutation CLINVAR Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function. 22835832

2012
dbSNP: rs74315368
rs74315368
SDHB
T 0.800 CausalMutation CLINVAR Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations. 21173220

2011
dbSNP: rs74315372
rs74315372
SDHB
G 0.800 CausalMutation CLINVAR

dbSNP: rs772551056
rs772551056
SDHB
T 0.800 GeneticVariation CLINVAR Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. 16317055

2006
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 GeneticVariation CLINVAR Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function. 22835832

2012
dbSNP: rs772551056
rs772551056
SDHB
A 0.800 GeneticVariation CLINVAR

dbSNP: rs772551056
rs772551056
SDHB
T 0.800 CausalMutation CLINVAR Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function. 22835832

2012
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 CausalMutation CLINVAR R46Q mutation in the succinate dehydrogenase B gene (SDHB) in a Japanese family with both abdominal and thoracic paraganglioma following metastasis. 18362451

2008
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 CausalMutation CLINVAR Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer. 23083876

2012
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2015
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 GeneticVariation CLINVAR Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444

2013
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 GeneticVariation CLINVAR Biochemically silent abdominal paragangliomas in patients with mutations in the succinate dehydrogenase subunit B gene. 18840642

2008
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 GeneticVariation CLINVAR SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery. 26719882

2016
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 CausalMutation CLINVAR Immunohistochemical loss of succinate dehydrogenase subunit A (SDHA) in gastrointestinal stromal tumors (GISTs) signals SDHA germline mutation. 23282968

2013
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 CausalMutation CLINVAR SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery. 26719882

2016
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 CausalMutation CLINVAR Genetic testing in pheochromocytoma or functional paraganglioma. 16314641

2005
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 CausalMutation CLINVAR Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. 14500403

2003
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 CausalMutation CLINVAR Genetic mutation screening in an italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients. 17102082

2006
dbSNP: rs772551056
rs772551056
SDHB
T 0.800 GeneticVariation CLINVAR Clinicopathological study of SDHB mutation-related pheochromocytoma and sympathetic paraganglioma. 24659481

2014