| | | Single nucleotide variant (missense variant) | Hearing loss, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hidrotic ectodermal dysplasia syndrome +3 more | |
| | | Deletion | Autosomal recessive nonsyndromic hearing loss 1B | |
| | | Deletion | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Duplication | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1B +3 more | |
| | | Single nucleotide variant (missense variant) | Hidrotic ectodermal dysplasia syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1B +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +5 more | |
| | | Duplication (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 1B +5 more | |
| | | Deletion | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +5 more | |
| | | Copy number loss | Autosomal recessive nonsyndromic hearing loss 1B | |
| | | Single nucleotide variant (missense variant) | Hidrotic ectodermal dysplasia syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hidrotic ectodermal dysplasia syndrome +4 more | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 1B +4 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1B +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | LOC130009329, LOC132090175 +32 more | Duplication | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1B +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | GJB6-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1B +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Hidrotic ectodermal dysplasia syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1B +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hidrotic ectodermal dysplasia syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +5 more | |
| | | Duplication (frameshift variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hidrotic ectodermal dysplasia syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | Hidrotic ectodermal dysplasia syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hidrotic ectodermal dysplasia syndrome +5 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +12 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3A +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Deletion | Autosomal recessive nonsyndromic hearing loss 1A +5 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Rare genetic deafness +10 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive nonsyndromic hearing loss 104 +14 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Palmoplantar keratoderma-deafness syndrome +14 more | |
| | | Deletion | Nonsyndromic genetic hearing loss | |
| | | Deletion (frameshift variant) | Nonsyndromic genetic hearing loss | |
| | | Deletion | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Palmoplantar keratoderma-deafness syndrome +12 more | |
| | | Single nucleotide variant (nonsense) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (nonsense) | not provided +10 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Deletion | Autosomal recessive nonsyndromic hearing loss 1B +2 more | |
| | | Single nucleotide variant (missense variant) | Hidrotic ectodermal dysplasia syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | GJB6-related disorder +6 more | |