Disease: Neoplastic Syndromes, Hereditary ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs876658367
rs876658367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies. 24781345 2014
dbSNP: rs876658367
rs876658367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		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
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		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
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR Bilateral adrenal medullary hyperplasia associated with an SDHB mutation. 21172883 2011
dbSNP: rs876658367
rs876658367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582 2009
dbSNP: rs876658367
rs876658367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		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
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		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
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas. 17652212 2007
dbSNP: rs876658367
rs876658367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. 16317055 2006
dbSNP: rs876658367
rs876658367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		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
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR Genetic testing in pheochromocytoma or functional paraganglioma. 16314641 2005
dbSNP: rs876658367
rs876658367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. 15328326 2004
dbSNP: rs876658367
rs876658367
Entrez Id: 6390
Gene Symbol: SDHB
SDHB
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 CausalMutation CLINVAR Germ-line mutations in nonsyndromic pheochromocytoma. 12000816 2002