| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126806658, CTNNB1 (E15D +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CTNNB1, LOC126806658 (M202T +1 more) | Single nucleotide variant (missense variant) | not provided | |
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