| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FBXO11, LOC100506235 (Q42R) | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities +1 more | GConflicting classifications of pathogenicity |
| | FBXO11, LOC100506235 (P36L) | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities +1 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene