| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129994026, PTCD2 (R11L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC129994026, PTCD2 (S34F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC129994026, PTCD2 (P12R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC129994026, PTCD2 (Q22P) | Single nucleotide variant (missense variant +1 more) | not specified | |
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