RAD51

RAD51 recombinase
OMIM: 179617
PanelMode of inheritanceDetails
4 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
R-numbers: R21, R412
Signed-off version 4.195
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Fanconi anaemia, complementation group R, OMIM:617244
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 6.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Fanconi anemia, complementation group R, OMIM:617244
R-numbers: R88
Signed-off version 6.8
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Fanconi anemia, complementation group R, OMIM:617244