Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398123690
rs398123690
SDHB
C 0.700 CausalMutation CLINVAR Genetics of Apparently Sporadic Pheochromocytoma and Paraganglioma in a Chinese Population. 26267327

2015