| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Wolfram-like syndrome +4 more | GPathogenic/Likely pathogenic |
| | GREB1L, LOC101927521 (T116I) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss | |
Click to view in NCBI Gene