Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs377767406
rs377767406
RET
T 0.700 CausalMutation CLINVAR Patients with RET D631Y mutations most commonly present with pheochromocytoma and not medullary thyroid carcinoma. 22274720

2012
dbSNP: rs377767406
rs377767406
RET
T 0.700 CausalMutation CLINVAR Medullary thyroid cancer: management guidelines of the American Thyroid Association. 19469690

2009
dbSNP: rs377767406
rs377767406
RET
T 0.700 CausalMutation CLINVAR Familial prevalence and age of RET germline mutations: implications for screening. 18062802

2008
dbSNP: rs377767406
rs377767406
RET
T 0.700 CausalMutation CLINVAR A rare extracellular D631Y germline mutation of the RET proto-oncogene in two Korean families with multiple endocrine neoplasia 2A. 16839264

2006
dbSNP: rs377767406
rs377767406
RET
T 0.700 CausalMutation CLINVAR A patient with MEN 2 and multiple mutations of RET in the germline. 11149622

2000
dbSNP: rs377767406
rs377767406
RET
T 0.700 CausalMutation CLINVAR Mechanism of Ret activation by a mutation at aspartic acid 631 identified in sporadic pheochromocytoma. 10049754

1999
dbSNP: rs377767406
rs377767406
RET
T 0.700 CausalMutation CLINVAR The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects. 7608256

1995