Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs377767406
rs377767406
RET
0.030 GeneticVariation BEFREE Patients with MEN2A caused by a D631Y RET mutation most commonly present with pheochromocytomas. 28747092

2017
dbSNP: rs377767406
rs377767406
RET
0.030 GeneticVariation BEFREE Patients with a D631Y RET mutation typically present with pheochromocytoma and medullary thyroid carcinoma appears to occur with a later onset than reported with other RET mutations. 22274720

2012
dbSNP: rs377767406
rs377767406
RET
0.030 GeneticVariation BEFREE In addition, pheochromocytoma might be the first manifestation prior to the development of MTC in some patients with the D631Y mutation. 16839264

2006