| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC109611589, RUNX2 (A59E +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC109611589, RUNX2 (A65V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene