Gene: MIR4658 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 100616439
Gene Symbol: MIR4658
MIR4658 		0.010 GeneticVariation disease BEFREE The T>C variant of rs1317082 at CCSlnc362 exon 1 created a binding site for miR-4658 to reduce the expression of CCSlnc362 and thus decreased the susceptibility to CRC. 30518759 2018