| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861663, MLXIP (D240H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MLXIP, LOC126861663 (S287P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene