| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC127814297, POU4F3 (A189fs) | Duplication (frameshift variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (L248P) | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (F293L) | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (V318M) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
Click to view in NCBI Gene