| | | Single nucleotide variant (missense variant +1 more) | not provided +5 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) | Colorectal cancer, hereditary nonpolyposis, type 2 +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) | Hereditary breast ovarian cancer syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Hereditary nonpolyposis colorectal neoplasms +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | not specified +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome | |
| | | 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 (missense variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome | |