| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC120977025, PTPRN (A792T +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC120977025, PTPRN (F872Y +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC120977025, PTPRN (T861N +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC120977025, PTPRN (V859G +2 more) | Single nucleotide variant (missense variant) | not specified | |
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