| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Duplication (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | LOC130060418, MYO15A (W3136C) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (splice acceptor variant) | not provided +1 more | |
| | | Duplication (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | LOC130060418, MYO15A (R3134P) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | LOC130060418, MYO15A (R3134*) | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Duplication (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Duplication (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (inframe_deletion) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (splice donor variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (inframe_deletion) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Microsatellite (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Duplication (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (inframe_deletion) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Microsatellite (inframe_deletion) | Autosomal recessive nonsyndromic hearing loss 3 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 3 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 3 | |