| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Microsatellite (intron variant) | Autosomal dominant nonsyndromic hearing loss 41 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant nonsyndromic hearing loss 41 +2 more | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant nonsyndromic hearing loss 41 +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
Click to view in NCBI Gene