| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Duplication | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion | not provided | |
| | | Deletion | Cataract 14 multiple types | |
Click to view in NCBI Gene