| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | COCH, LOC100506071 (T352S +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal dominant nonsyndromic hearing loss 9 +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
Click to view in NCBI Gene