rs9330814

This variant is located in the WNT7B gene.

GWAS Catalog Trait Associations (5)

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

hematocrit

Allele T
OR 0.02
p 2.0e-69
N 928,679
Large GWAS
multi-ancestry
Allele T
OR
p 8.0e-62
N 737,823
Large GWAS
multi-ancestry

erythrocyte count

Allele T
OR 0.02
p 4.0e-65
N 928,679
Large GWAS
multi-ancestry
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.03
p 6.0e-43
N 503,987
Large GWAS
multi-ancestry
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele T
OR 0.03
p 2.0e-33
N 408,112
Large GWAS
European

red blood cell density

Allele T
OR
p 9.0e-57
N 727,624
Large GWAS
multi-ancestry

colorectal cancer

Allele T
OR 0.05
p 2.0e-9
N 254,791
Large GWAS
multi-ancestry

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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