| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CD163L1, LOC126861436 (G1278D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861436, CD163L1 (A1264S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CD163L1, LOC126861436 (E1264K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene