| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 79 | |
| | LOC130003092, TMEM203 +1 more (E101*) | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 79 | |
| | | Duplication (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 79 +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 79 +2 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 79 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 79 | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 79 | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 79 +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 79 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Microsatellite (inframe_deletion) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 79 | |
| | | Microsatellite (frameshift variant) | not provided +2 more | |
| | | Duplication (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 79 | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 79 | |
| | | Single nucleotide variant (nonsense) | Hearing loss, autosomal recessive +1 more | GPathogenic/Likely pathogenic |