| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | PNPLA4, LOC125446266 (E57A) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC125446266, PNPLA4 (A40S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC125446266, PNPLA4 (C26Y) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene