| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Diabetes insipidus, nephrogenic, autosomal | |
| | | Single nucleotide variant (intron variant) | Diabetes insipidus, nephrogenic, autosomal | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |
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