| | | Single nucleotide variant (missense variant) | Hearing loss, autosomal recessive | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hidrotic ectodermal dysplasia syndrome +3 more | |
| | | Duplication (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Duplication (inframe_insertion) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Deletion | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Duplication | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (nonsense) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1B +3 more | |
| | | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 1A +1 more | |
| | | Single nucleotide variant (missense variant) | Hidrotic ectodermal dysplasia syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1B +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1B +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Deletion (inframe_deletion) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +5 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Indel (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Duplication (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 1B +5 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (synonymous variant) | Knuckle pads, deafness AND leukonychia syndrome +8 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +8 more | |
| | | Deletion | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Hearing impairment +10 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +5 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 1A | |
| | | Single nucleotide variant (5 prime UTR variant) | Knuckle pads, deafness AND leukonychia syndrome +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (missense variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (missense variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Knuckle pads, deafness AND leukonychia syndrome +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Ichthyosis, hystrix-like, with hearing loss +2 more | |
| | | Single nucleotide variant (missense variant) | Hidrotic ectodermal dysplasia syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hidrotic ectodermal dysplasia syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 3A +2 more | |
| | | Deletion (frameshift variant) | Autosomal recessive nonsyndromic hearing loss 1B +4 more | |
| | | Deletion (frameshift variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1B +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 1A +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 3B +3 more | |
| | LOC130009329, LOC132090175 +32 more | Duplication | Autosomal recessive nonsyndromic hearing loss 1A +3 more | |
| | | Deletion (frameshift variant) | Nonsyndromic genetic hearing loss +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 1A | |