| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | CTNNB1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | CTNNB1-related disorder +2 more | |
| | CTNNB1, LOC126806659 (R462H +1 more) | Single nucleotide variant (missense variant) | Severe intellectual disability-progressive spastic diplegia syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | CTNNB1-related disorder +1 more | |
Click to view in NCBI Gene