| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Werner syndrome | |
| | | Single nucleotide variant (intron variant) | Werner syndrome | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Werner syndrome | |
| | | Deletion (intron variant) | Werner syndrome | |
| | | Single nucleotide variant (missense variant) | Werner syndrome | |
| | | Single nucleotide variant (nonsense) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice acceptor variant) | Werner syndrome | |
| | | Single nucleotide variant (missense variant) | Werner syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Werner syndrome | |
| | | Single nucleotide variant (missense variant) | Werner syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (splice donor variant) | Werner syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Werner syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Ovarian cancer +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Indel (missense variant) | Werner syndrome | |
| | | Deletion (frameshift variant) | WRN-related disorder +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Werner syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Werner syndrome | |
| | | Single nucleotide variant (splice donor variant) | Werner syndrome | |
| | | Single nucleotide variant (splice acceptor variant) | Werner syndrome | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Werner syndrome | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Werner syndrome | |
| | | Single nucleotide variant (missense variant) | Werner syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Werner syndrome | |
| | | Single nucleotide variant (intron variant) | Werner syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Werner syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Werner syndrome | |
| | | Single nucleotide variant (missense variant) | Werner syndrome | GConflicting classifications of pathogenicity |