rs79658334, RET

N. diseases: 29
Disease: Pheochromocytoma ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
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
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
0.710 CausalMutation CLINVAR