Gene: LRP6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4040
Gene Symbol: LRP6
LRP6 		0.010 GeneticVariation disease BEFREE Thus, mutation Y418H in LRP6 likely contributes to normolipidemic familial CAD via impairing endothelial cell functions and weakening the Wnt3a signaling pathway. 27455246 2016