Non-Fanconi anaemia
Gene: FANCI
Variants in this GENE are reported as part of current diagnostic practice
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Fanconi anemia complementation group I
FANCI was added to Non-Fanconi anaemiapanel. Source: Expert list
Model of inheritance for gene FANCI was set to BIALLELIC, autosomal or pseudoautosomal
FANCI was added to Non-Fanconi anaemiapanel. Source: UKGTN
Model of inheritance for gene FANCI was set to BIALLELIC, autosomal or pseudoautosomal
FANCI was added to Non-Fanconi anaemiapanel. Source: Radboud University Medical Center, Nijmegen
Model of inheritance for gene FANCI was set to BIALLELIC, autosomal or pseudoautosomal
FANCI was added to Non-Fanconi anaemiapanel. Source: Illumina TruGenome Clinical Sequencing Services
Model of inheritance for gene FANCI was set to BIALLELIC, autosomal or pseudoautosomal
FANCI was added to Non-Fanconi anaemiapanel. Source: UKGTN
Model of inheritance for gene FANCI was set to BIALLELIC, autosomal or pseudoautosomal
FANCI was added to Non-Fanconi anaemiapanel. Source: Radboud University Medical Center, Nijmegen
Model of inheritance for gene FANCI was set to BIALLELIC, autosomal or pseudoautosomal
FANCI was added to Non-Fanconi anaemiapanel. Source: Illumina TruGenome Clinical Sequencing Services
Model of inheritance for gene FANCI was changed to BIALLELIC, autosomal or pseudoautosomal
FANCI was added to Non-Fanconi anaemiapanel. Sources: Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN
Model of inheritance for gene FANCI was changed to BIALLELIC, autosomal or pseudoautosomal
FANCI was added to Non-Fanconi anaemiapanel. Sources: Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN
FANCI was added to Non-Fanconi anaemiapanel. Sources: Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN