| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | GREB1L, LOC101927521 (R328*) | Single nucleotide variant (nonsense) | Inner ear malformation +1 more | |
| | | Single nucleotide variant (missense variant) | Hearing loss, autosomal dominant 80 +1 more | |
Click to view in NCBI Gene