Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201286421
rs201286421
T 0.700 CausalMutation CLINVAR Polymyalgia rheumatica and vagal paraganglioma. 28412079

2017

dbSNP: rs201286421
rs201286421
T 0.700 CausalMutation CLINVAR Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients. 27279923

2016

dbSNP: rs201286421
rs201286421
T 0.700 CausalMutation CLINVAR Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies. 24781345

2014

dbSNP: rs201286421
rs201286421
T 0.700 CausalMutation CLINVAR The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3). 24758179

2014

dbSNP: rs201286421
rs201286421
T 0.700 CausalMutation CLINVAR Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes. 22703879

2012

dbSNP: rs201286421
rs201286421
T 0.700 CausalMutation CLINVAR Long-delayed localization of a cardiac functional paraganglioma with SDHC mutation. 22868853

2012

dbSNP: rs201286421
rs201286421
T 0.700 CausalMutation CLINVAR Synchronous carotid body and thoracic paraganglioma associated with a germline SDHC mutation. 21106325

2011

dbSNP: rs201286421
rs201286421
T 0.700 CausalMutation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582

2009

dbSNP: rs201286421
rs201286421
T 0.700 CausalMutation CLINVAR Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. 17667967

2008