Table 2.
Genetic Mutations | Family Syndromes |
---|---|
BRCA1/BRCA2 | Hereditary breast and ovarian cancer syndrome |
PALB2 | Hereditary syndrome related to PALB2 mutation |
MLH1, MSH2, MSH6, PMS2 | Lynch syndrome |
TP53 | Li-Fraumeni syndrome |
CDKN2A/p16 | Familial atypical multiple mole melanoma syndrome |
STK11 | Peutz-Jeghers syndrome |
PRSS1 | Hereditary pancreatitis syndrome |