Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122805
rs398122805
SDHB
T 0.700 CausalMutation CLINVAR Phenotype of SDHB mutation carriers in the Netherlands. 25047027

2014
dbSNP: rs398122805
rs398122805
SDHB
T 0.700 CausalMutation CLINVAR High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands. 21348866

2012
dbSNP: rs398122805
rs398122805
SDHB
T 0.700 CausalMutation CLINVAR Low penetrance of a SDHB mutation in a large Dutch paraganglioma family. 20540712

2010
dbSNP: rs398122805
rs398122805
SDHB
T 0.700 CausalMutation CLINVAR Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients. 19825962

2009
dbSNP: rs398122805
rs398122805
SDHB
T 0.700 CausalMutation CLINVAR Malignant extra-adrenal pheochromocytoma caused by an SDHB intronic variation leading to a 54-bp deletion in exon 4. 19411806

2009
dbSNP: rs398122805
rs398122805
SDHB
T 0.700 CausalMutation CLINVAR Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma. 16405730

2006