| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic Hearing Loss, Recessive +5 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (splice acceptor variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +2 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | CDH23-related disorder +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pituitary adenoma 5, multiple types +3 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +5 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +3 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +5 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +3 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +3 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +4 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +2 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +3 more | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic genetic hearing loss | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +5 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +3 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +4 more | |
| | | Single nucleotide variant (missense variant) | CDH23-related disorder +5 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +4 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | CDH23-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Pituitary adenoma 5, multiple types +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Pituitary adenoma 5, multiple types +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Usher syndrome type 1D +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Usher syndrome type 1D +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Usher syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | CDH23-related disorder +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Usher syndrome | |
| | | Indel (splice acceptor variant +1 more) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Rare genetic deafness +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Usher syndrome type 1D +4 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 12 +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Pituitary adenoma 5, multiple types +4 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome | |
| | | Single nucleotide variant (missense variant) | Usher syndrome +9 more | |
| | | Single nucleotide variant (nonsense) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +4 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Beta-D-mannosidosis +4 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +4 more | |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Rare genetic deafness +4 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +3 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 12 +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +3 more | |
| | | Single nucleotide variant (missense variant) | CDH23-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Pituitary adenoma 5, multiple types +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Usher syndrome type 1D +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |