Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs75076352
rs75076352
RET
0.710 GeneticVariation BEFREE MEN2A patients are affected by RET (C634Y, C634R) mutation; MEN2B patients are affected by RET (M918T) mutation. 29237911

2017
dbSNP: rs75076352
rs75076352
RET
C 0.710 GeneticVariation CLINVAR RET activation by germline MEN2A and MEN2B mutations. 8570194

1995