Variant: rs10453441 

    present in Gene: WNT7B
    present in Chromosome: 22
    Position on Chromosome: 45967859
    Alleles of this Variant: A/G

rs10453441 in WNT7B gene and Central corneal thickness PMID 29847655 2018 Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus.

PMID 28171582 2016 Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos.

rs10453441 in WNT7B gene and Corneal Topography PMID 25823570 2015 Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia.