| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130001484, PLPP6
+1 more (G30D) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130001484, PLPP6
+1 more (A48G) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130001484, PLPP6
+1 more (P96A) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
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