| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126860893, MPP7 (L306M) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | MPP7, LOC126860893 (R302Q) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126860893, MPP7 (I288M) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126860893, MPP7 (S266N) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126860893, MPP7 (Y239F) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
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