| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126805634, PADI6 (P199R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126805634, PADI6 (R207W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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