| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Usher syndrome type 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +2 more | |
| | | Single nucleotide variant (non-coding transcript variant +2 more) | Usher syndrome type 3 | |
| | | Single nucleotide variant (non-coding transcript variant +2 more) | Hearing impairment +1 more | |
Click to view in NCBI Gene