In addition, we confirm variants with pathogenic status in BRCA1 and BRCA2 as they were never encountered in homozygosity except in two cases with resulting Fanconi anemia phenotype (NM_ 000059.3:c.7007G > A:p.Arg2336His and NM_000059.3: c.9152delC, p.Pro3051Hisfs*11). This evidence concerns the gene BRCA2 and Fanconi anemia.