Variant: rs9330813 

    present in Gene: WNT7B
    present in Chromosome: 22
    Position on Chromosome: 45968281
    Alleles of this Variant: G/A;C

rs9330813 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.

rs9330813 in WNT7B gene and Hematocrit procedure PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs9330813 in WNT7B gene and Red Blood Cell Count measurement PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.