| | | Deletion | Autosomal dominant nonsyndromic hearing loss 3A +5 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 provided +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | GJB2-related disorder +12 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +2 more | |
| | | Deletion | Nonsyndromic genetic hearing loss +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +11 more | GPathogenic/Likely pathogenic |
| | | Duplication | not provided +11 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Ichthyosis, hystrix-like, with hearing loss +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Deletion | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (nonsense) | not provided +10 more | |
| | | Single nucleotide variant (missense variant) | not provided +13 more | |
| | | Deletion (frameshift variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | 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 +1 more) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (splice acceptor variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | GJB2-related disorder +15 more | GPathogenic/Likely pathogenic |