Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607032
rs267607032
A 0.700 GeneticVariation CLINVAR The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers. 28503760

2018

dbSNP: rs397516836
rs397516836
A 0.700 CausalMutation CLINVAR Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD. 29386252

2018

dbSNP: rs398122805
rs398122805
T 0.700 CausalMutation CLINVAR The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers. 28503760

2018

dbSNP: rs772551056
rs772551056
T 0.700 CausalMutation CLINVAR The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers. 28503760

2018

dbSNP: rs786202732
rs786202732
G 0.700 CausalMutation CLINVAR The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers. 28503760

2018

dbSNP: rs267607032
rs267607032
A 0.700 GeneticVariation CLINVAR SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations. 28374168

2017

dbSNP: rs267607032
rs267607032
A 0.700 GeneticVariation CLINVAR The phenotype of SDHB germline mutation carriers: a nationwide study. 28490599

2017

dbSNP: rs587782604
rs587782604
T 0.700 CausalMutation CLINVAR Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling. 27604842

2017

dbSNP: rs74315366
rs74315366
A 0.700 CausalMutation CLINVAR SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations. 28374168

2017

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

2017

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

2017

dbSNP: rs772551056
rs772551056
T 0.700 CausalMutation CLINVAR SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations. 28374168

2017

dbSNP: rs772551056
rs772551056
T 0.700 CausalMutation CLINVAR The phenotype of SDHB germline mutation carriers: a nationwide study. 28490599

2017

dbSNP: rs786201095
rs786201095
C 0.700 CausalMutation CLINVAR SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations. 28374168

2017

dbSNP: rs200245469
rs200245469
A 0.700 GeneticVariation CLINVAR Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome. 26960314

2016

dbSNP: rs397516834
rs397516834
A 0.700 GeneticVariation CLINVAR Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients. 27279923

2016

dbSNP: rs397516836
rs397516836
A 0.700 CausalMutation CLINVAR Rapid-sequence MRI for long-term surveillance for paraganglioma and phaeochromocytoma in patients with succinate dehydrogenase mutations. 27634942

2016

dbSNP: rs397516836
rs397516836
A 0.700 CausalMutation CLINVAR Carney triad can be (rarely) associated with germline succinate dehydrogenase defects. 26173966

2016

dbSNP: rs398122805
rs398122805
T 0.700 CausalMutation CLINVAR Sporadic paraganglioma caused by de novo SDHB mutations in a 6-year-old girl. 26283294

2016

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

2016

dbSNP: rs772551056
rs772551056
T 0.700 CausalMutation CLINVAR SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery. 26719882

2016

dbSNP: rs772551056
rs772551056
T 0.700 CausalMutation CLINVAR A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGL. 27700540

2016

dbSNP: rs786201161
rs786201161
C 0.700 CausalMutation CLINVAR Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathy. 26642834

2016

dbSNP: rs786202732
rs786202732
G 0.700 CausalMutation CLINVAR Mediastinal paragangliomas related to SDHx gene mutations. 27785149

2016

dbSNP: rs1278834014
rs1278834014
A 0.700 GeneticVariation CLINVAR 15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5. 26273102

2015