Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799939
rs1799939
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C4722172
Disease:
Primary differentiated carcinoma of thyroid gland
0.010 GeneticVariation BEFREE Subgroup analysis showed that concomitant thyroid benign diseases were less likely to occur in DTC subjects with the rs1799939 AG or AG plus AA genotypes (odds ratio (OR) = 1.93 and 1.88, P = 0.009 and 0.011, respectively). 29131865 2017