| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC123956210, SLC26A4 (I700V) | Single nucleotide variant (missense variant) | not provided | |
| | LOC123956210, SLC26A4 (T721M) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 4 +3 more | |
| | LOC123956210, SLC26A4 (D724G) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 4 +4 more | GPathogenic/Likely pathogenic |
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