| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Insertion (inframe_insertion) | Autosomal recessive nonsyndromic hearing loss 9 | |
| | OTOF, LOC112840921 (R1013L +2 more) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 9 | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal recessive nonsyndromic hearing loss 9 | |
Click to view in NCBI Gene