WNT7B, Wnt family member 7B, 7477

N. diseases: 53; N. variants: 5
Disease: Central corneal thickness ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness 		0.100 GeneticVariation phenotype GWASCAT Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus. 29847655 2018
CUI: C1720164
Disease: Central corneal thickness
Central corneal thickness 		0.100 GeneticVariation phenotype GWASCAT Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos. 28171582 2016