| | | Single nucleotide variant (nonsense) | Rare genetic deafness +5 more | |
| | | Single nucleotide variant (nonsense) | Usher syndrome type 1 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Usher syndrome type 1F +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal recessive nonsyndromic hearing loss 23 | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Pituitary adenoma 5, multiple types +1 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Usher syndrome | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +1 more | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (splice donor variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Pituitary adenoma 5, multiple types +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Usher syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant +1 more) | Pituitary adenoma 5, multiple types +1 more | |
| | | Single nucleotide variant (nonsense) | Rare genetic deafness +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +1 more | |
| | | Deletion (frameshift variant) | Pituitary adenoma 5, multiple types +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +9 more | |
| | | Single nucleotide variant (nonsense) | Pituitary adenoma 5, multiple types +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Rare genetic deafness +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Rare genetic deafness +4 more | |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Usher syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Pituitary adenoma 5, multiple types +1 more | |
| | | Single nucleotide variant (synonymous variant) | Rare genetic deafness +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Usher syndrome type 1 +2 more | |
| | LOC111982869, CDH23 (F2664del +1 more) | Microsatellite (inframe_deletion) | Pituitary adenoma 5, multiple types +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Retinal dystrophy +2 more | |
| | | Duplication (frameshift variant) | Pituitary adenoma 5, multiple types +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Usher syndrome | |
| | | Deletion (frameshift variant) | Pituitary adenoma 5, multiple types +2 more | |
| | | Deletion (frameshift variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +4 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +3 more | |
| | | Single nucleotide variant (splice acceptor variant) | Usher syndrome type 1C +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant +1 more) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice acceptor variant) | Autosomal recessive nonsyndromic hearing loss 18A +1 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive nonsyndromic hearing loss 18A +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Usher syndrome type 1C +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant +1 more) | Rare genetic deafness +6 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Rare genetic deafness +5 more | |
| | | Single nucleotide variant (nonsense +1 more) | Usher syndrome type 1C +3 more | |
| | | Single nucleotide variant (splice donor variant) | Rare genetic deafness +3 more | |
| | | Deletion (frameshift variant) | Usher syndrome type 1 | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice acceptor variant) | not provided +4 more | |
| | | Deletion (frameshift variant) | Usher syndrome type 1 | |
| | | Single nucleotide variant (missense variant) | Usher syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 11 +2 more | |
| | | Deletion (frameshift variant) | Rare genetic deafness +4 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Rare genetic deafness +3 more | GPathogenic/Likely pathogenic |