RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Disease: C-cell hyperplasia of thyroid ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs377767404
rs377767404
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0342190
Disease:
C-cell hyperplasia of thyroid 		0.010 GeneticVariation BEFREE There was considerable variability of malignant progression from C-cell hyperplasia to MTC in carriers of the Cys630Arg genotype. 15523405 2004