| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Rare genetic deafness +3 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 +2 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene