Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74799832
rs74799832
RET
C 0.800 CausalMutation CLINVAR Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma. 10445857

1999
dbSNP: rs74799832
rs74799832
RET
0.800 GeneticVariation BEFREE Small MTC in C634R may be less aggressive than those in C634Y and M918T. 9839497

1998
dbSNP: rs74799832
rs74799832
RET
C 0.800 GeneticVariation CLINVAR C618S developed late onset type of MTC as compared with that of C634R, C634Y and M918T. 9839497

1998
dbSNP: rs74799832
rs74799832
RET
0.800 GeneticVariation BEFREE Apart from the MET918-->Thr mutation in 5 of the MTC cases, we found a 3-bp deletion in exon 11, only present in the tumor, in another case. 8768845

1996