| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Pendred syndrome | |
| | LOC123956210, SLC26A4 (H723R) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 4 +4 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene