| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CEACAM16, CEACAM16-AS1 (R235C) | Single nucleotide variant (missense variant) | Hearing loss, autosomal recessive 113 +1 more | GConflicting classifications of pathogenicity |
| | CEACAM16, CEACAM16-AS1 (T236K) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
Click to view in NCBI Gene