| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC123956210, SLC26A4 (T721M) | Single nucleotide variant (missense variant) | Rare genetic deafness +3 more | |
| | LOC123956210, SLC26A4 (H723R) | Single nucleotide variant (missense variant) | Rare genetic deafness +4 more | GPathogenic/Likely pathogenic |
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