| | | Deletion (frameshift variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Kidney disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | Kidney disorder | |
| | | Single nucleotide variant (synonymous variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Kidney disorder | |
| | | Deletion (5 prime UTR variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant +1 more) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Nephronophthisis-like nephropathy 1 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Atypical hemolytic-uremic syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | | Microsatellite (inframe_deletion) | Atypical hemolytic-uremic syndrome | |
| | | Deletion (frameshift variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | CD46, LOC129932405 (L28fs) | Deletion (frameshift variant) | Atypical hemolytic-uremic syndrome | |
| | | Deletion (frameshift variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Atypical hemolytic-uremic syndrome | |
| | | Deletion (intron variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (synonymous variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (synonymous variant) | Atypical hemolytic-uremic syndrome | |
| | | Microsatellite (inframe_deletion) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (synonymous variant) | Kidney disorder +5 more | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (synonymous variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (synonymous variant) | Kidney disorder | |
| | | Single nucleotide variant (synonymous variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (intron variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | | Single nucleotide variant (missense variant) | Atypical hemolytic-uremic syndrome | |
| | NPHP3-ACAD11, NPHP3 (N653S) | Single nucleotide variant (missense variant) | Kidney disorder | |
| | NPHP3-ACAD11, NPHP3 (I681R) | Single nucleotide variant (non-coding transcript variant +1 more) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Kidney disorder | |
| | | Single nucleotide variant (intron variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (synonymous variant) | Kidney disorder | |
| | | Single nucleotide variant (synonymous variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (synonymous variant) | Focal segmental glomerulosclerosis 5 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Kidney disorder | |
| | | Single nucleotide variant (splice donor variant) | Kidney disorder +1 more | |
| | | Single nucleotide variant (nonsense) | Kidney disorder | |
| | | Deletion (frameshift variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (intron variant) | Kidney disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (intron variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |
| | | Duplication (5 prime UTR variant +1 more) | Focal segmental glomerulosclerosis | |
| | AXDND1, NPHS2 (P248R +1 more) | Single nucleotide variant (missense variant +1 more) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (intron variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (intron variant) | Focal segmental glomerulosclerosis +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (synonymous variant) | Focal segmental glomerulosclerosis +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis +1 more | |
| | | Single nucleotide variant (missense variant) | Kidney disorder | |
| | | Single nucleotide variant (intron variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (synonymous variant) | CD2AP-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Focal segmental glomerulosclerosis +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |
| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis | |