| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC127814297, POU4F3 (P135S) | Single nucleotide variant (missense variant) | not specified +2 more | |
| | LOC127814297, POU4F3 (S171R) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 +3 more | |
Click to view in NCBI Gene