| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | AXDND1, NPHS2 (A297V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Focal segmental glomerulosclerosis +6 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene