| | | Single nucleotide variant (3 prime UTR variant) | Nonsyndromic genetic hearing loss +5 more | GConflicting classifications of pathogenicity |
| | | Deletion | Rare genetic deafness +5 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant) | GJB2-related condition +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss +12 more | GPathogenic/Likely pathogenic |
| | | Indel | Rare genetic deafness +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3A +6 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Ear malformation +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss +10 more | |
| | | Single nucleotide variant (missense variant) | GJB2-related condition +12 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +11 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +6 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (inframe_deletion) | Hearing impairment +11 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Deletion | Nonsyndromic genetic hearing loss +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +11 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3A +14 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +12 more | |
| | | Deletion | Nonsyndromic genetic hearing loss | |
| | | Deletion (frameshift variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Hearing impairment | |
| | | Single nucleotide variant (nonsense) | X-linked mixed hearing loss with perilymphatic gusher +11 more | |
| | | Single nucleotide variant (nonsense) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss +5 more | |
| | | Single nucleotide variant (nonsense) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | not provided +11 more | GPathogenic/Likely pathogenic |
| | | Deletion | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive nonsyndromic hearing loss 1A +15 more | GPathogenic/Likely pathogenic |