| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 2A +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Microsatellite (inframe_insertion) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant nonsyndromic hearing loss 2A +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Deletion (inframe_deletion) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 2A +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (splice acceptor variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Microsatellite (inframe_deletion) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Microsatellite (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 2A +3 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Autosomal dominant nonsyndromic hearing loss 2A +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Deletion | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | KCNQ4-related disorder +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | KCNQ4, LOC129930282 (F182L) | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 2A +1 more | |
| | | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 2A | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |