Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397514034
rs397514034
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Diagnosis and management of hereditary paraganglioma syndrome due to the F933>X67 SDHD mutation. 19072999

2009
dbSNP: rs397514034
rs397514034
SDHD ; TIMM8B
A 0.700 CausalMutation CLINVAR Germline SDHD mutation in familial phaeochromocytoma. 11323050

2001