WNT7B, Wnt family member 7B, 7477

N. diseases: 53; N. variants: 5
Disease: Corneal Topography ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10453441
rs10453441
Entrez Id: 7477
Gene Symbol: WNT7B
WNT7B
CUI: C0524957
Disease:
Corneal Topography 		A 0.700 GeneticVariation GWASCAT Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. 25823570 2015