Table 1.

Genes associated with Fanconi anemia

Gene% of FA casesInheritancePopulation distribution and unique phenotypes
FANCA 45-60 AR Founder mutations: Middle Eastern, North African, Spanish Romani, Afrikaner, Sicilian
Mutation-specific disease severity 
FANCC 10-15 AR Founder mutations: Ashkenazi, Saudi, northern Europe
Exon 15 mutations: more severe phenotype
c.67delG: milder phenotype 
FANCG 5-10 AR Founder mutations: Sub-Saharan Africa, Japan, Korea
Severe hematologic disease 
FANCB 1-2 XL VACTERL-H common 
FANCD1/BRCA2 1-4 AR High leukemia risk: myeloid and lymphoid
Early childhood solid tumors: brain, Wilms, neuroblastoma
Aplastic BMF uncommon
Carriers: risk of breast, ovarian, prostate, pancreatic cancer 
FANCD2 3-5 AR Sequencing challenging due to pseudogenes 
FANCI 1-4 AR VACTERL-H common 
FANCJ/BRIP1 1-4 AR Carriers: increased breast/ovarian cancer risk 
FANCL 1-2 AR Founder mutations: India, Pakistan
VACTERL-H common 
FANCM <2 AR Lower risk of congenital anomalies and BMF
Early-onset cancer risk 
FANCN/PALB2 <2 AR Severe clinical presentation
High leukemia risk
Early childhood solid tumors: brain, Wilms, neuroblastoma
Carriers: breast and pancreatic cancer risk 
FANCQ/ERCC4 <2 AR Overlap with xeroderma pigmentosum 
FANCR/RAD51 <2 AD Congenital anomalies common
BMF and cancer not yet reported 
FANCS/BRCA1 <2 AR Severe solid tumor and leukemia risk
Congenital anomalies
BMF not yet reported
Carriers: risk of breast, ovarian, prostate, pancreatic cancer 
FANCE, FANCF, FANCO, FANCP, FANCT, FANCU, FANCV, FANCW, FANCY <2 AR Rare cases only 
Gene% of FA casesInheritancePopulation distribution and unique phenotypes
FANCA 45-60 AR Founder mutations: Middle Eastern, North African, Spanish Romani, Afrikaner, Sicilian
Mutation-specific disease severity 
FANCC 10-15 AR Founder mutations: Ashkenazi, Saudi, northern Europe
Exon 15 mutations: more severe phenotype
c.67delG: milder phenotype 
FANCG 5-10 AR Founder mutations: Sub-Saharan Africa, Japan, Korea
Severe hematologic disease 
FANCB 1-2 XL VACTERL-H common 
FANCD1/BRCA2 1-4 AR High leukemia risk: myeloid and lymphoid
Early childhood solid tumors: brain, Wilms, neuroblastoma
Aplastic BMF uncommon
Carriers: risk of breast, ovarian, prostate, pancreatic cancer 
FANCD2 3-5 AR Sequencing challenging due to pseudogenes 
FANCI 1-4 AR VACTERL-H common 
FANCJ/BRIP1 1-4 AR Carriers: increased breast/ovarian cancer risk 
FANCL 1-2 AR Founder mutations: India, Pakistan
VACTERL-H common 
FANCM <2 AR Lower risk of congenital anomalies and BMF
Early-onset cancer risk 
FANCN/PALB2 <2 AR Severe clinical presentation
High leukemia risk
Early childhood solid tumors: brain, Wilms, neuroblastoma
Carriers: breast and pancreatic cancer risk 
FANCQ/ERCC4 <2 AR Overlap with xeroderma pigmentosum 
FANCR/RAD51 <2 AD Congenital anomalies common
BMF and cancer not yet reported 
FANCS/BRCA1 <2 AR Severe solid tumor and leukemia risk
Congenital anomalies
BMF not yet reported
Carriers: risk of breast, ovarian, prostate, pancreatic cancer 
FANCE, FANCF, FANCO, FANCP, FANCT, FANCU, FANCV, FANCW, FANCY <2 AR Rare cases only 

Data derived from Fanconi Anemia Clinical Care Guidelines.

AD, autosomal dominant; AR, autosomal recessive; VACTERL-H, vertebral, anal, cardiac, tracheoesophageal fistula, esophageal atresia, renal, limb, hydrocephalus; XL, X-linked.

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