Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 724029
Gene Symbol: MIR659
MIR659
0.020 GeneticVariation disease BEFREE This is consistent with the finding that miR-659 binding to the high risk T allele of rs5848 may augment translational inhibition of GRN and alter risk of FTD and possibly other dementias. 21047645 2011
Entrez Id: 724029
Gene Symbol: MIR659
MIR659
0.020 GeneticVariation disease BEFREE Here we expand the role of GRN in FTLD-U and demonstrate that a common genetic variant (rs5848), located in the 3'-untranslated region (UTR) of GRN in a binding-site for miR-659, is a major susceptibility factor for FTLD-U. 18723524 2008