Lynch Syndrome: PREMM 1,2,6 Model - (full access - calculator)

PREMM 1,2,6 Model | index

Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer)

PREMM_1,2,6 Model: Prediction Model for MLH1, MSH2, and MSH6 Gene Mutations

The PREMM_1,2,6 model is a clinical prediction algorithm designed for use by healthcare professionals to estimate the cumulative and individual probabilities that an individual is an MLH1, MSH2, or MSH6 mutation carrier. Mutations in these genes are found in most patients with Lynch syndrome.