Data for: Machine learning-based genetic diagnosis models for hereditary hearing loss by the GJB2, SLC26A4 and MT-RNR1 variants

This is the Supporting Datasets for the manuscript "Machine learning-based genetic diagnosis models for hereditary hearing loss by the GJB2, SLC26A4 and MT-RNR1 variants" by Luo et al in EBiomedicine .
The two data sets were processed sequencing data, of which the Discovery Set was from the medical records and the Validation Set was from the Disabled Persons' Federation.
PS: No mutations found were indicated by 0, heterozygous mutations by 1, and homozygous mutations by 2