| | | Single nucleotide variant (3 prime UTR variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Deletion | Hearing impairment +5 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant) | Hearing impairment +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +12 more | GPathogenic/Likely pathogenic |
| | | Indel | Rare genetic deafness +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified +6 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 1A +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +10 more | |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +12 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +6 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (inframe_deletion) | Nonsyndromic genetic hearing loss +11 more | |
| | | Single nucleotide variant (missense variant) | not specified +9 more | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Deletion | Autosomal recessive nonsyndromic hearing loss 1A +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Palmoplantar keratoderma-deafness syndrome +12 more | |
| | | Deletion | Nonsyndromic genetic hearing loss | |
| | | Deletion (frameshift variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 1A +11 more | |
| | | Single nucleotide variant (nonsense) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Single nucleotide variant (nonsense) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | not provided +11 more | GPathogenic/Likely pathogenic |
| | | Deletion | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive nonsyndromic hearing loss 1A +15 more | GPathogenic/Likely pathogenic |