| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | GREB1L, LOC101927521 (T383fs +1 more) | Deletion (frameshift variant) | Renal hypodysplasia/aplasia 3 | |
| | | Single nucleotide variant (intron variant) | Renal hypodysplasia/aplasia 3 | |
| | | Single nucleotide variant (missense variant) | Renal hypodysplasia/aplasia 3 | |
| | | Deletion (frameshift variant) | Renal hypodysplasia/aplasia 3 | |
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