| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC109611589, RUNX2 (Q57del +1 more) | Microsatellite (inframe deletion +1 more) | RUNX2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Microsatellite (inframe_deletion) | Cleidocranial dysostosis +2 more | |
| | LOC109611589, RUNX2 (A75del +1 more) | Microsatellite (inframe deletion +1 more) | RUNX2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Cleidocranial dysostosis +2 more | |
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