| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC106780803, TNXB (R4169H +2 more) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
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