WNT7B, Wnt family member 7B, 7477

N. diseases: 53; N. variants: 5
Disease: Corneal Topography ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		0.100 GeneticVariation phenotype GWASCAT Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. 25823570 2015