| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Microsatellite (frameshift variant) | not provided +5 more | |
| | | Duplication (nonsense) | Lynch syndrome | |
| | FBXO11, MSH6 (D826G +1 more) | Single nucleotide variant (missense variant) | Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene