rs10919908
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.
age at onset, Myopia
Tedja MS et al. “Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.” Nature Genetics 50(6):834-848 (2018)
Allele A
OR 0.05
p 7.0e-12
N 104,293
Meta-analysisLarge 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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