| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | INPP1, LOC129935252 (A19V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | INPP1, LOC129935252 (Q24fs) | Deletion (frameshift variant) | Cleft palate +1 more | |
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