| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC123956210, SLC26A4 (T721K) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 4 | |
| | LOC123956210, SLC26A4 (H723D) | Single nucleotide variant (missense variant) | Pendred syndrome +2 more | |
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