| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | SLX1B, SLX1B-SULT1A4 (P201S +2 more) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | SLX1B, SLX1B-SULT1A4 (C236F +3 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | SLX1B, SLX1B-SULT1A4 (E160G +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene