| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC127814297, POU4F3 (S23fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (H109Y) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (G160fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
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