Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs916516745
rs916516745
T 0.700 CausalMutation CLINVAR

dbSNP: rs397516835
rs397516835
T 0.700 CausalMutation CLINVAR Effect of cysteine to serine mutations on the properties of the [4Fe-4S] center in Escherichia coli fumarate reductase. 7547971

1995

dbSNP: rs786202732
rs786202732
G 0.700 CausalMutation CLINVAR Effect of cysteine to serine mutations on the properties of the [4Fe-4S] center in Escherichia coli fumarate reductase. 7547971

1995

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

2001

dbSNP: rs74315367
rs74315367
C 0.700 GeneticVariation CLINVAR Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. 11404820

2001

dbSNP: rs397516835
rs397516835
T 0.700 CausalMutation CLINVAR Crystallographic studies of the Escherichia coli quinol-fumarate reductase with inhibitors bound to the quinol-binding site. 11850430

2002

dbSNP: rs794728947
rs794728947
TG 0.700 CausalMutation CLINVAR Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. 11897817

2002

dbSNP: rs587781266
rs587781266
T 0.700 CausalMutation CLINVAR Germ-line mutations in nonsyndromic pheochromocytoma. 12000816

2002

dbSNP: rs74315370
rs74315370
C 0.700 CausalMutation CLINVAR Germ-line mutations in nonsyndromic pheochromocytoma. 12000816

2002

dbSNP: rs786202732
rs786202732
G 0.700 CausalMutation CLINVAR Germ-line mutations in nonsyndromic pheochromocytoma. 12000816

2002

dbSNP: rs876658367
rs876658367
T 0.700 CausalMutation CLINVAR Germ-line mutations in nonsyndromic pheochromocytoma. 12000816

2002

dbSNP: rs74315369
rs74315369
A 0.700 CausalMutation CLINVAR SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation. 12362046

2002

dbSNP: rs74315367
rs74315367
C 0.700 GeneticVariation CLINVAR Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma. 12364472

2002

dbSNP: rs772551056
rs772551056
T 0.700 CausalMutation CLINVAR Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma. 12364472

2002

dbSNP: rs1131691060
rs1131691060
T 0.700 CausalMutation CLINVAR Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. 12618761

2003

dbSNP: rs74315370
rs74315370
A 0.700 CausalMutation CLINVAR Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. 12618761

2003

dbSNP: rs747198089
rs747198089
T 0.700 CausalMutation CLINVAR Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. 12618761

2003

dbSNP: rs876659329
rs876659329
T 0.700 GeneticVariation CLINVAR Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. 12618761

2003

dbSNP: rs876659330
rs876659330
G 0.700 GeneticVariation CLINVAR Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. 12618761

2003

dbSNP: rs138996609
rs138996609
A 0.700 CausalMutation CLINVAR Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. 14500403

2003

dbSNP: rs74315370
rs74315370
C 0.700 CausalMutation CLINVAR Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. 14500403

2003

dbSNP: rs587781266
rs587781266
T 0.700 CausalMutation CLINVAR Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma. 14685938

2004

dbSNP: rs74315369
rs74315369
A 0.700 CausalMutation CLINVAR Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma. 14685938

2004

dbSNP: rs74315368
rs74315368
T 0.700 CausalMutation CLINVAR The prevalence of SDHB, SDHC, and SDHD mutations in patients with head and neck paraganglioma and association of mutations with clinical features. 15235042

2004

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR The prevalence of SDHB, SDHC, and SDHD mutations in patients with head and neck paraganglioma and association of mutations with clinical features. 15235042

2004