| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 4B | |
| | CEACAM16-AS1, CEACAM16 (T82M) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 4B | |
Click to view in NCBI Gene