| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | INPPL1, LOC130006328 (L34R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | INPPL1, LOC130006328 (D48N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | INPPL1, LOC130006328 (C59G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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