| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126859748, PNISR (D411G +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126859748, PNISR (S390F +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126859748, PNISR (S387A +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
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