| | | Single nucleotide variant (3 prime UTR variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Duplication (frameshift variant) | Pierson syndrome | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Deletion (inframe_deletion) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (nonsense) | LAMB2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related infantile-onset nephrotic syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Indel (missense variant) | Pierson syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (splice donor variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (splice donor variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Pierson syndrome +1 more | |
| | | Microsatellite (frameshift variant) | LAMB2-related disorder | |
| | | Microsatellite (frameshift variant) | LAMB2-related infantile-onset nephrotic syndrome | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Duplication (frameshift variant) | Pierson syndrome | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | LAMB2-related infantile-onset nephrotic syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Pierson syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | LAMB2-related infantile-onset nephrotic syndrome +2 more | |