RAD51

RAD51 recombinase
OMIM: 179617
PanelMode of inheritanceDetails
3 panels
R-numbers: R229, R258
Signed-off version 2.5
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Fanconi anemia, complementation group R, OMIM:617244
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.13
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Fanconi anemia, complementation group R, OMIM:617244
R-numbers: R88
Signed-off version 4.41
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Fanconi anemia, complementation group R, OMIM:617244