| | | Deletion | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Duplication (frameshift variant +1 more) | Lynch syndrome 1 +1 more | |
| | | Duplication | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Duplication | Hereditary nonpolyposis colorectal neoplasms | |
| | | Duplication | Hereditary nonpolyposis colorectal neoplasms | |
| | | Duplication | Hereditary nonpolyposis colorectal neoplasms | |
| | | Duplication | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Deletion | Hereditary nonpolyposis colorectal neoplasms | |
| | | Copy number loss | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +3 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 1 | |
| | | Indel (inframe_indel +2 more) | Lynch syndrome 1 | |
| | | Indel (frameshift variant +2 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (intron variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | KCNK12, LOC129933697 +1 more (C401Y) | Single nucleotide variant (intron variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 1 | |
| | | Deletion (inframe_deletion +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (nonsense +1 more) | Lynch syndrome 1 | |
| | | Deletion | Lynch syndrome 1 | |
| | KCNK12, MSH2 (G449R +5 more) | Single nucleotide variant (missense variant +2 more) | Hereditary cancer | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +3 more) | not provided | |
| | | Duplication (frameshift variant +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (intron variant) | Lynch syndrome 1 | |
| | | Duplication (frameshift variant +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +2 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Duplication (frameshift variant +2 more) | not provided | |
| | | Deletion (splice acceptor variant +1 more) | Lynch syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | Ovarian cancer | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | KCNK12, LOC129933697 +1 more (S357R) | Single nucleotide variant (missense variant) | not specified | |
| | KCNK12, LOC129933697 +1 more (D358A) | Single nucleotide variant (missense variant) | not specified | |
| | KCNK12, LOC129933697 +1 more (D356A) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Deletion | not provided | |
| | | Microsatellite (frameshift variant) | not provided | |
| | | Deletion | not provided | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Insertion | Hereditary cancer-predisposing syndrome | |
| | | Duplication | Hereditary nonpolyposis colon cancer | |
| | | Indel (frameshift variant) | Lynch syndrome 1 | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Deletion | Lynch syndrome 1 | |
| | | Duplication | Hereditary cancer-predisposing syndrome | |
| | | Deletion (frameshift variant) | not provided | |
| | | Duplication | Lynch syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary cancer-predisposing syndrome | |