rs3213787
This is a intron variant variant in the SRBD1 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.
glaucoma
Meguro A et al. “Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility.” Ophthalmology 117(7):1331-8.e5 (2010)
Allele A
OR 2.80
p 3.0e-9
N 660
Small GWAS
East Asian
About SRBD1
Predicted to enable mRNA binding activity. Predicted to be a structural constituent of ribosome. Predicted to be involved in translation. [provided by Alliance of Genome Resources, Jul 2025]
View all SRBD1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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