| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129996783, ZNF292 (G14S) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC129996783, ZNF292 (G16A) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC129996783, ZNF292 (A20T) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC129996783, ZNF292 (Q23P) | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +1 more | |
Click to view in NCBI Gene