| | | Single nucleotide variant (5 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary nonpolyposis colorectal neoplasms +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary nonpolyposis colorectal neoplasms +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | MSH6-related condition +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Lynch syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Hereditary nonpolyposis colorectal neoplasms +3 more | |
| | | Duplication (frameshift variant) | MSH6-related condition +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +1 more | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome 5 +3 more | |
| | | Single nucleotide variant (splice acceptor variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Lynch syndrome 5 +4 more | |
| | | Single nucleotide variant (nonsense) | Lynch syndrome | |
| | | Duplication (inframe_insertion) | not specified +4 more | |
| | | Deletion (frameshift variant) | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary nonpolyposis colorectal neoplasms +2 more | GConflicting classifications of pathogenicity |