| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CRBN, TRNT1 (R419* +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | not provided | GConflicting classifications of pathogenicity |
| | CRBN, TRNT1 (C391R +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Intellectual disability, autosomal recessive 2 +1 more | |
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