Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 GeneticVariation disease BEFREE Genetic screening revealed a succinate dehydrogenase complex subunit C (SDHC) germline mutation, confirming hereditary paraganglioma/pheochromocytoma syndrome. 29501297 2018
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR Vascular Endothelial Growth Factor Receptor-Targeted Therapy in Succinate Dehydrogenase C Kidney Cancer. 25024072 2016
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 GeneticVariation disease CLINVAR Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients. 27279923 2016
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGL. 27700540 2016
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 GeneticVariation disease CLINVAR Toward an improved definition of the genetic and tumor spectrum associated with SDH germ-line mutations. 25394176 2015
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 GeneticVariation disease CLINVAR Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. 24728327 2014
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 GeneticVariation disease CLINVAR Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas. 24102379 2014
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR Phenotypic variability and risk of malignancy in SDHC-linked paragangliomas: lessons from three unrelated cases with an identical germline mutation (p.Arg133*). 24423348 2014
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3). 24758179 2014
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR Pheochromocytoma and paraganglioma syndromes: genetics and management update. 24523625 2014
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies. 24781345 2014
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 GeneticVariation disease CLINVAR Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444 2013
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 GeneticVariation disease CLINVAR A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma. 23666964 2013
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444 2013
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes. 22703879 2012
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer. 23083876 2012
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR Long-delayed localization of a cardiac functional paraganglioma with SDHC mutation. 22868853 2012
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma. 21784903 2011
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR Synchronous carotid body and thoracic paraganglioma associated with a germline SDHC mutation. 21106325 2011
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 GeneticVariation disease CLINVAR Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out. 19351833 2009
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582 2009
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease 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
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 CausalMutation disease CLINVAR Germline mutations in PTEN and SDHC in a woman with epithelial thyroid cancer and carotid paraganglioma. 17898811 2007
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma. 16405730 2006
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. 16249420 2005