Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs79658334
rs79658334
RET
0.710 GeneticVariation BEFREE This clinical case suggests that individuals carrying the germline V804M mutation should be screened annually for the presence of pheochromocytoma. 17466010

2007
dbSNP: rs79658334
rs79658334
RET
A 0.710 CausalMutation CLINVAR