| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130004825, SFXN4 (E35K) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | LOC130004825, SFXN4 (N28S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130004825, SFXN4 (P22S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene