Adult solid tumours for rare diseaseGene: MSH2
Tumor Suppressor. Biallelic phenotype.
Created: 5 Jul 2017, 12:19 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Lynch Syndrome; CMMRD
5th March 2018 - promoted to version 1 after expert review and internal clinical review.
MSH2 was added to Adult solid tumours for rare disease panel. Sources: Expert list,Expert Review Green
MSH2 was created by Ellen McDonagh