| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130061961, OXLD1 (R13G +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC130061961, OXLD1 (A22V +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
Click to view in NCBI Gene