| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CEACAM16, CEACAM16-AS1 (S32I) | Indel (missense variant) | Autosomal dominant nonsyndromic hearing loss 4B +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hearing loss, autosomal recessive 113 +3 more | |
| | CEACAM16, CEACAM16-AS1 (R379W) | Single nucleotide variant (missense variant) | Hearing impairment +2 more | |
| | CEACAM16, CEACAM16-AS1 (D397E) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 4B +2 more | |
Click to view in NCBI Gene