| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity; association; risk factor |
| | | Single nucleotide variant (intron variant) | Finnish congenital nephrotic syndrome +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene