| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense +1 more) | not provided +3 more | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome | |
| | | Single nucleotide variant (splice acceptor variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Deletion (splice acceptor variant +2 more) | Lynch syndrome | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome | |
| | | Duplication (frameshift variant) | Lynch syndrome | |
| | | Single nucleotide variant (splice donor variant) | Lynch syndrome | |
| | | Indel (splice donor variant) | Lynch syndrome | |
| | | Single nucleotide variant (synonymous variant) | Lynch syndrome | |
| | | Deletion (splice acceptor variant +2 more) | Colorectal cancer, hereditary nonpolyposis, type 2 | |
| | | Duplication (frameshift variant +1 more) | Lynch syndrome | |
| | | Deletion (frameshift variant +1 more) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome | |
| | | Deletion (frameshift variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome +4 more | |
| | | Duplication (frameshift variant) | Lynch syndrome | |
| | | Deletion (frameshift variant) | Lynch syndrome 1 | |
| | | Duplication (frameshift variant +1 more) | Lynch syndrome | |