| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130063246, LOC130063247
+810 more | Copy number gain | See cases | |
| | LOC130063377, PNPLA6 (M1T) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
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