| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ABCC3, LOC125177504 (E1459Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCC3, LOC125177504 (V1434M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCC3, LOC125177504 (R1442C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene