| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hearing loss, autosomal recessive 109 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hearing loss, autosomal recessive 109 +1 more | |
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