| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | SLC26A4, SLC26A4-AS1 (M1T) | Single nucleotide variant (non-coding transcript variant +2 more) | Autosomal recessive nonsyndromic hearing loss 4 +4 more | |
| | | Single nucleotide variant (missense variant) | Pendred syndrome | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 4 +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Pendred syndrome | |
| | | Single nucleotide variant (missense variant) | SLC26A4-related disorder +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene