| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Microsatellite (intron variant) | Familial juvenile hyperuricemic nephropathy type 2 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Renal tubular dysgenesis of genetic origin +4 more | |
| | | Single nucleotide variant (intron variant) | Familial juvenile hyperuricemic nephropathy type 2 +2 more | |
| | | Single nucleotide variant (missense variant) | Familial juvenile hyperuricemic nephropathy type 2 +2 more | |
| | | Single nucleotide variant (nonsense) | Familial juvenile hyperuricemic nephropathy type 2 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Renal tubular dysgenesis of genetic origin +1 more | |
| | LOC107548112, REN (L16del) | Microsatellite (inframe_deletion) | Renal tubular dysgenesis of genetic origin +2 more | GPathogenic/Likely pathogenic |
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