rs111811307

This variant is located in the KIAA0232 gene.

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ClinVar annotation

Likely Benign
1 submitter

KIAA0232-related disorder

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About KIAA0232

Predicted to enable ATP binding activity. [provided by Alliance of Genome Resources, Jul 2025]

View all KIAA0232 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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