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Inherited MMR deficiency (Lynch syndrome) v1.6 MSH2 Arina Puzriakova Phenotypes for gene: MSH2 were changed from to Colorectal cancer, hereditary nonpolyposis, type 1, OMIM:120435; Lynch syndrome 1, MONDO:0007356
Inherited MMR deficiency (Lynch syndrome) v0.11 MSH2 Ivone Leong commented on gene: MSH2
Inherited MMR deficiency (Lynch syndrome) v0.7 MSH2 Ivone Leong Mode of inheritance for gene: MSH2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Inherited MMR deficiency (Lynch syndrome) v0.3 MSH2 Rachel Robinson reviewed gene: MSH2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Inherited MMR deficiency (Lynch syndrome) v0.3 MSH2 Lara Hawkes reviewed gene: MSH2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Inherited MMR deficiency (Lynch syndrome) v0.2 MSH2 Ivone Leong gene: MSH2 was added
gene: MSH2 was added to Inherited MMR deficiency (Lynch syndrome). Sources: Expert List,Expert Review Green,NHS GMS
Mode of inheritance for gene: MSH2 was set to