| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 21 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant nonsyndromic hearing loss 21 +2 more | |
| | | Deletion | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (splice donor variant) | Rare genetic deafness +14 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene