| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Nonsyndromic Hearing Loss, Dominant +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (intron variant) | Nonsyndromic Hearing Loss, Dominant | |
Click to view in NCBI Gene