| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126653398, TSPEAR
+1 more (Y566C +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 98 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
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