Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057517818
rs1057517818
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553265817
rs1553265817
C 0.700 CausalMutation CLINVAR

dbSNP: rs587776653
rs587776653
C 0.700 CausalMutation CLINVAR

dbSNP: rs786202200
rs786202200
A 0.700 GeneticVariation CLINVAR

dbSNP: rs786205146
rs786205146
C 0.700 CausalMutation CLINVAR

dbSNP: rs867966048
rs867966048
C 0.700 GeneticVariation CLINVAR

dbSNP: rs876658301
rs876658301
GT 0.700 CausalMutation CLINVAR

dbSNP: rs981049067
rs981049067
A 0.700 CausalMutation CLINVAR

dbSNP: rs587778661
rs587778661
T 0.700 GeneticVariation CLINVAR A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma. 23666964

2013

dbSNP: rs786203457
rs786203457
G 0.700 GeneticVariation CLINVAR A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma. 23666964

2013

dbSNP: rs764575966
rs764575966
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: rs764575966
rs764575966
T 0.700 CausalMutation CLINVAR Adrenocortical carcinoma and succinate dehydrogenase gene mutations: an observational case series. 28819017

2017

dbSNP: rs764575966
rs764575966
T 0.700 CausalMutation CLINVAR AN AGGRESSIVE TEMPORAL BONE SDHC PARAGANGLIOMA ASSOCIATED WITH INCREASED HIF-2α SIGNALING. 26492543

2016

dbSNP: rs587776653
rs587776653
T 0.700 CausalMutation CLINVAR Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. 12658451

2003

dbSNP: rs786205147
rs786205147
A 0.700 GeneticVariation CLINVAR Carney triad can be (rarely) associated with germline succinate dehydrogenase defects. 26173966

2016

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

dbSNP: rs587778661
rs587778661
T 0.700 GeneticVariation CLINVAR Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out. 19351833

2009

dbSNP: rs755235380
rs755235380
G 0.700 CausalMutation CLINVAR Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out. 19351833

2009

dbSNP: rs786205147
rs786205147
A 0.700 GeneticVariation CLINVAR Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out. 19351833

2009

dbSNP: rs898854295
rs898854295
G 0.700 GeneticVariation CLINVAR Crystal structure of mitochondrial respiratory membrane protein complex II. 15989954

2005

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

2014

dbSNP: rs764575966
rs764575966
T 0.700 CausalMutation CLINVAR Germline mutations in PTEN and SDHC in a woman with epithelial thyroid cancer and carotid paraganglioma. 17898811

2007

dbSNP: rs786203457
rs786203457
G 0.700 GeneticVariation CLINVAR Germline SDHC mutation presenting as recurrent SDH deficient GIST and renal carcinoma. 24150194

2013

dbSNP: rs587778661
rs587778661
T 0.700 GeneticVariation CLINVAR Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. 24728327

2014

dbSNP: rs786203457
rs786203457
G 0.700 GeneticVariation CLINVAR Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort. 25494863

2015