rs34320898

This is a intron variant variant in the METTL13 gene.

GWAS Catalog Trait Associations (2)

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

platelet component distribution width

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.03
p 2.0e-32
N 408,112
Large GWAS
European

intelligence

Allele C
OR 5.95
p 3.0e-9
N 269,867
Meta-analysisLarge GWAS
European

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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