| Panel | Mode of inheritance | Details |
|---|---|---|
5 panels | ||
Signed-off version 2.2 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Familial Adenomatous Polyposis |
Green in APC associated PolyposisR-numbers: R414 Signed-off version 1.4 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Desmoid disease, hereditary, OMIM:135290, Adenomatous polyposis coli, OMIM:175100, Brain tumor-polyposis syndrome 2, OMIM:175100, Gardner syndrome, OMIM:175100, Gastric adenocarcinoma and proximal polyposis of the stomach, OMIM:619182, desmoid tumor, MONDO:0007608, gastric adenocarcinoma and proximal polyposis of the stomach, MONDO:0017790, familial adenomatous polyposis 1, MONDO:0021056 |
Signed-off version 1.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Adult Glioma |
Green in Childhood solid tumoursSigned-off version 5.11 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Familial Adenomatous Polyposis, 175100 |
R-numbers: R211 Signed-off version 4.2 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Desmoid disease, hereditary, OMIM:135290, Brain tumor-polyposis syndrome 2, OMIM:175100, Gardner syndrome, OMIM:175100, Adenomatous polyposis coli, OMIM:175100, Gastric adenocarcinoma and proximal polyposis of the stomach, OMIM:619182 |