| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130004501, NKX2-3 (A227T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130004501, NKX2-3 (G235R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130004501, NKX2-3 (P263S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene