| | | Single nucleotide variant (missense variant) | Focal segmental glomerulosclerosis +4 more | |
| | | Single nucleotide variant (nonsense) | LAMB2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Microsatellite (frameshift variant) | LAMB2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Focal segmental glomerulosclerosis +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related disorder +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder +2 more | |
| | | Single nucleotide variant (intron variant) | Pierson syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | LAMB2-related infantile-onset nephrotic syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related disorder | |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Focal segmental glomerulosclerosis +4 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | Pierson syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related infantile-onset nephrotic syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | LAMB2-related disorder | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (intron variant) | LAMB2-related disorder +2 more | |
| | | Deletion (frameshift variant) | LAMB2-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Pierson syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | LAMB2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related disorder | |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related disorder +4 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Pierson syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | Pierson syndrome +2 more | GConflicting classifications of pathogenicity |