| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130061928, NDUFAF8 (V7L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130061928, NDUFAF8 (R10C) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene