rs145666727

This variant is located in the METTL13 gene.

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ClinVar annotation

Risk Factor

1 submitter1 publication

Deafness, autosomal recessive 26, modifier of

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]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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