rs1536478
This is a intron variant variant in the LOC100506532 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
central corneal thickness
Gao X et al. “Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos.” Human Molecular Genetics 25(22):5035-5045 (2016)
Allele G
OR 4.17
p 2.0e-8
N 3,584
Large GWAS
Hispanic or Latin American
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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