| | | Single nucleotide variant (splice donor variant) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Single nucleotide variant (nonsense +1 more) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 22 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Duplication (nonsense +1 more) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Indel (nonsense +1 more) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 22 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant nonsyndromic hearing loss 22 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +3 more | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | | Duplication (nonsense +1 more) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant nonsyndromic hearing loss 22 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 22 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal dominant nonsyndromic hearing loss 22 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 37 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 22 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Deletion (frameshift variant +1 more) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (nonsense +1 more) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Duplication (frameshift variant +1 more) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 22 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal recessive nonsyndromic hearing loss 37 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | |