rs10453441

This variant is located in the WNT7B gene.

GWAS Catalog Trait Associations (3)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

corneal topography

Allele A
OR 0.05
p 3.0e-40
N 3,248
Large GWAS
multi-ancestry

central corneal thickness

Allele G
OR 3.11
p 2.0e-11
N 210
Small GWAS
multi-ancestry
Allele G
OR 4.51
p 6.0e-9
N 3,584
Large GWAS
Hispanic or Latin American

About WNT7B

This gene is a member of the WNT gene family, which consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. Among members of the human WNT family, this gene product is most similar to WNT7A protein. [provided by RefSeq, Oct 2008]

View all WNT7B variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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