| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FBXO11, MSH6 (S747G +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Deletion (intron variant) | not specified | |
| | | Microsatellite (intron variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
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