Pathogenic variants (disease-causing) in the MSH2 gene cause Lynch syndrome (previously known as hereditary non-polyposis colorectal cancer (HNPCC)). People with pathogenic variants in MSH2 have a high lifetime risk for primarily colorectal cancer and endometrial (uterine) cancer in women. Individuals also have increased risks for other Lynch syndrome-associated cancers, including ovarian, gastrointestinal tumors (stomach, small bowel, pancreas), urinary tract (kidney, ureter, bladder), prostate, skin (sebaceous [oil gland] tumors), and brain cancer. Management of MSH2–related tumor risk includes regular surveillance tailored to guidelines to detect tumors early as well as risk-reducing strategies (surgery and medication). MSH2 variants are known to be more common in the Ashkenazi Jewish population.
Pathogenic variants in MSH2 exhibit autosomal dominant inheritance. This means there is a 50% chance the condition can be passed from generation-to-generation. First degree relatives (parents, siblings, children) have a 50% chance to have the same pathogenic variant whereas second degree relatives (grandparents, aunts/uncles, nieces/nephews, half-siblings) have a 25% chance. More distant relatives have lower chances of having the same pathogenic variant when one is identified in the family.
In addition, when an individual inherits pathogenic variants in both copies of the MSH2 gene or one copy of the MSH2 gene and one copy of the EPCAM gene (which also causes Lynch syndrome), it can cause a rare childhood-onset condition called constitutional mismatch repair deficiency (CMMRD). CMMRD results in a risk of childhood onset cancers including colon cancer and leukemia as well as features of a genetic condition called neurofibromatosis type 1 which causes benign skin tumors. CMMRD exhibits autosomal recessive inheritance. This means that both parents must be have a single pathogenic variant in the MSH2 gene or again, one in MSH2 and one in EPCAM, to have a 25% chance to have a child with the condition.
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Written December 2025
