| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC107372315, OSGEP (I53F) | Single nucleotide variant (missense variant) | Galloway-Mowat syndrome 3 | |
| | LOC107372315, OSGEP (N27K) | Single nucleotide variant (missense variant) | Galloway-Mowat syndrome 3 | |
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