| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130057886, PLIN1 (P462L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130057886, PLIN1 (A459T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130057886, PLIN1 (G442S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130057886, PLIN1 (G437V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130057886, PLIN1 (S436P) | Single nucleotide variant (missense variant) | not specified | |
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