| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC124416936, PAOX (G297S +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC124416936, PAOX (P300L) | Single nucleotide variant (synonymous variant +2 more) | Inborn genetic diseases | |
| | LOC124416936, PAOX (R408W) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
Click to view in NCBI Gene