| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129994296, SLCO4C1 (I19S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129994296, SLCO4C1 (P17L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129994296, SLCO4C1 (P39T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Copy number loss | not specified | |
Click to view in NCBI Gene