WNT7B, Wnt family member 7B, 7477

N. diseases: 53; N. variants: 5
Disease: Central corneal thickness ×
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: C1720164
Disease:
Central corneal thickness 		G 0.700 GeneticVariation GWASCAT Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus. 29847655 2018
dbSNP: rs10453441
rs10453441
Entrez Id: 7477
Gene Symbol: WNT7B
WNT7B
CUI: C1720164
Disease:
Central corneal thickness 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos. 28171582 2016