Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs751000085
rs751000085
SDHB
A 0.700 CausalMutation CLINVAR The phenotype of SDHB germline mutation carriers: a nationwide study. 28490599

2017
dbSNP: rs751000085
rs751000085
SDHB
A 0.700 CausalMutation CLINVAR Phenotype of SDHB mutation carriers in the Netherlands. 25047027

2014
dbSNP: rs751000085
rs751000085
SDHB
A 0.700 CausalMutation CLINVAR Pheochromocytoma and paraganglioma syndromes: genetics and management update. 24523625

2014
dbSNP: rs751000085
rs751000085
SDHB
A 0.700 CausalMutation CLINVAR High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands. 21348866

2012
dbSNP: rs751000085
rs751000085
SDHB
A 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