| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 13 | |
| | | Single nucleotide variant (splice donor variant) | Autosomal dominant nonsyndromic hearing loss 13 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 53 +5 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 53 +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Otospondylomegaepiphyseal dysplasia, autosomal dominant +5 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 53 +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 13 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 13 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hearing impairment +2 more | |
| | | Microsatellite (frameshift variant) | Fibrochondrogenesis 2 | |
| | | Single nucleotide variant (intron variant) | not provided +5 more | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant nonsyndromic hearing loss 13 +5 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive nonsyndromic hearing loss 53 +5 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 13 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Stickler Syndrome, Dominant +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Fibrochondrogenesis 2 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +6 more | |
| | | Single nucleotide variant (intron variant) | not provided +6 more | |
| | | Single nucleotide variant (synonymous variant) | Otospondylomegaepiphyseal dysplasia, autosomal recessive +7 more | |
| | | Single nucleotide variant (missense variant) | Fibrochondrogenesis 2 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not specified +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Connective tissue disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Stickler Syndrome, Dominant +8 more | |
| | | Single nucleotide variant (missense variant) | Fibrochondrogenesis 2 +7 more | |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 13 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Otospondylomegaepiphyseal dysplasia, autosomal recessive +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Otospondylomegaepiphyseal dysplasia, autosomal recessive +7 more | |
| | | Single nucleotide variant (intron variant) | Otospondylomegaepiphyseal dysplasia, autosomal dominant +7 more | |
| | | Single nucleotide variant (synonymous variant) | Otospondylomegaepiphyseal dysplasia, autosomal dominant +7 more | |
| | | Single nucleotide variant (intron variant) | Otospondylomegaepiphyseal dysplasia, autosomal dominant +7 more | |
| | | Single nucleotide variant (synonymous variant) | Otospondylomegaepiphyseal dysplasia, autosomal dominant +7 more | |
| | | Single nucleotide variant (intron variant) | Otospondylomegaepiphyseal dysplasia, autosomal dominant +7 more | |
| | | Single nucleotide variant (synonymous variant) | Otospondylomegaepiphyseal dysplasia, autosomal dominant +7 more | |
| | | Single nucleotide variant (intron variant) | Otospondylomegaepiphyseal dysplasia, autosomal dominant +7 more | |
| | | Single nucleotide variant (nonsense) | not provided +5 more | |
| | | Single nucleotide variant (nonsense) | Otospondylomegaepiphyseal dysplasia, autosomal dominant +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 13 | |
| | | Single nucleotide variant (missense variant) | Rare genetic deafness +2 more | GPathogenic/Likely pathogenic |