"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 456183	NM_001018113.3(FANCB):c.2327C>T (p.Ala776Val)	FANCB (A776V)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group B +2 more	GConflicting classifications of pathogenicity
Select item 246612	NM_001018113.3(FANCB):c.1996G>A (p.Gly666Ser)	FANCB (G666S)	Single nucleotide variant (missense variant)	FANCB-related condition +4 more	GConflicting classifications of pathogenicity
Select item 246611	NM_001018113.3(FANCB):c.1769T>C (p.Phe590Ser)	FANCB (F590S)	Single nucleotide variant (missense variant)	FANCB-related condition +7 more	GConflicting classifications of pathogenicity
Select item 368024	NM_001018113.3(FANCB):c.1494G>T (p.Lys498Asn)	FANCB (K498N)	Single nucleotide variant (missense variant)	VACTERL association, X-linked, with or without hydrocephalus +4 more	GConflicting classifications of pathogenicity
Select item 1299898	NM_001018113.3(FANCB):c.1008T>A (p.Ser336Arg)	FANCB (S336R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 197175	NM_001018113.3(FANCB):c.989T>C (p.Ile330Thr)	FANCB (I330T)	Single nucleotide variant (missense variant)	FANCB-related condition +3 more	GConflicting classifications of pathogenicity

ClinVar