| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant +1 more) | Rare genetic deafness +5 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene