Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786203251
rs786203251
T 0.700 CausalMutation CLINVAR Structural and functional consequences of succinate dehydrogenase subunit B mutations. 25972245

2015

dbSNP: rs786203251
rs786203251
T 0.700 CausalMutation CLINVAR Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444

2013

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444

2013

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma. 23072324

2013

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas. 22517554

2012

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. 19454582

2009

dbSNP: rs786203251
rs786203251
T 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: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA. 17376234

2007

dbSNP: rs786203251
rs786203251
A 0.700 CausalMutation CLINVAR Paraganglioma syndrome: SDHB, SDHC, and SDHD mutations in head and neck paragangliomas. 17102086

2006

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