Table 1:
Genetic mutations | BRCA1, BRCA 2, CDKN2A/p16, ATM, PALB2, MLH1, MSH2, MSH6, PMS2, APC, STK11 |
Family history | Individuals with at least two affected blood relatives on the same side of the family, of whom at least one is an FDR to the individual |
Hereditary cancer syndromes | Familial atypical multiple mole melanoma syndrome Peutz Jeghers syndrome Li Fraumeni syndrome Lynch syndrome Familial adenomatous polyposis |
Other risk factors | Chronic pancreatitis Hereditary pancreatitis New-onset diabetes mellitus Obesity Smoking Alcohol |