| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129992055, TNIP2 (R145C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129992055, TNIP2 (V35I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129992055, TNIP2 (D141N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene