rs17650204

This variant is located in the METTL13 gene.

GWAS Catalog Trait Associations (1)

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

level of myocilin in blood

Allele G
OR 0.06
p 3.0e-13
N 47,745
Large GWAS
European

ClinVar annotation

Benign
1 submitter

METTL13-related disorder

View on ClinVar →

About METTL13

Enables protein-lysine N-methyltransferase activity. Predicted to be involved in methylation. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

View all METTL13 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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