rs2808485
This is a intron variant variant in the LINC00862 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.
Myopia
Xue Z et al. “Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank.” Ebiomedicine 82:104161 (2022)
Allele T
OR 0.07
p 8.0e-9
N 64,268
Meta-analysisMajor Consortium StudyLarge GWAS
European
About LINC00862
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
View all LINC00862 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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