| | | Single nucleotide variant (intron variant) | Autosomal dominant nonsyndromic hearing loss 36 | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 | |
| | | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 36 | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 36 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 36 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 36 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 +2 more | |
| | | Single nucleotide variant (splice donor variant) | Ear malformation +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 36 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 7 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 +4 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 7 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 36 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 36 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 7 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 +3 more | |
| | | Single nucleotide variant (intron variant) | Nonsyndromic Hearing Loss, Dominant +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 7 +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 36 | |
| | | Single nucleotide variant (nonsense) | Rare genetic deafness +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |