RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Disease: Familial medullary thyroid carcinoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1206969193
rs1206969193
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.010 GeneticVariation BEFREE Our investigation indicated that the RET p.S891A mutation combined with OSMR p.G513D may underlie a novel phenotype manifesting as FMTC and CA. 26356818 2015