PREMM1,2,6
Version 1

The PREMM1,2,6 has been developed as a pretest to decide whether patients suspected of having Lynch syndrome should be tested for germline mismatch repair gene mutations. "PREMM1,2,6" is a logistic regression model. It calculates the risk of having a mutation in the mismatch repair genes MLH1, MSH2 and MSH6 (for single genes and overall) based on the personal and familial cancer history of the proband (colorectal, endometrial, and other Lynch syndrome related cancers).

LHA ID: 7Q0CEYUJ46-2

1 item is associated with this Model:

Human Disease: Hereditary breast ovarian cancer syndrome

Model type: Not specified

Model format: R package

Execution or visualisation environment: Shiny

Model image: No image specified

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Kastrinos et al.

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Views: 2278

Created: 13th May 2019 at 14:12

Last updated: 27th Nov 2019 at 12:53

Last used: 27th Jun 2022 at 02:40

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Version 1 Created 13th May 2019 at 14:12 by Silke Zachariae

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