rs77724903, RET

N. diseases: 23
Disease: Paraganglioma ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Paraganglioma
CUI: C0030421
Disease: Paraganglioma
0.010 GeneticVariation BEFREE We present the case of a 38-yr-old man with a sporadic, multifocal pheochromocytoma and paraganglioma who was discovered to carry a Y791F germline mutation in exon 13 of the RET proto-oncogene. 16388093 2005