| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LRTOMT, TOMT (R58* +1 more) | Single nucleotide variant (nonsense +1 more) | Autosomal recessive nonsyndromic hearing loss 63 | GConflicting classifications of pathogenicity |
| | LRTOMT, TOMT (L27P +1 more) | Single nucleotide variant (missense variant +1 more) | Autosomal recessive nonsyndromic hearing loss 63 | |
| | ANAPC15, LRTOMT
+1 more (S167fs +2 more) | Duplication (frameshift variant +3 more) | Inborn genetic diseases +1 more | |
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