| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | SLC26A4, SLC26A4-AS1 (E15fs) | Deletion (non-coding transcript variant +1 more) | Hearing loss, autosomal recessive +1 more | GPathogenic/Likely pathogenic |
| | SLC26A4, SLC26A4-AS1 (K52*) | Single nucleotide variant (non-coding transcript variant +1 more) | Deafness +1 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene