| | | Single nucleotide variant (missense variant +1 more) | MLH1-related condition +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant +2 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | MLH1-related condition +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Breast and/or ovarian cancer +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary nonpolyposis colorectal neoplasms +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome | |
| | | Insertion (intron variant) | Hereditary nonpolyposis colorectal neoplasms | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |
| | | Single nucleotide variant (splice donor variant) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Hereditary nonpolyposis colorectal neoplasms +6 more | |
| | | Indel (missense variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Hereditary nonpolyposis colorectal neoplasms +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |