List of variants reported as uncertain significance for Fanconi anemia complementation group B by Illumina Laboratory Services, Illumina

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001018113.3(FANCB):c.*151A>G	rs1480015600	0.00011
NM_001018113.3(FANCB):c.-111A>G	rs185118376	0.00009
NM_001018113.3(FANCB):c.-230A>T	rs1020271259	0.00008
NM_001018113.3(FANCB):c.196A>C (p.Thr66Pro)	rs943801800	0.00002
NM_001018113.3(FANCB):c.2327C>T (p.Ala776Val)	rs761492600	0.00002
NM_001018113.3(FANCB):c.1179T>C (p.Pro393=)	rs764156696	0.00001
NM_001018113.3(FANCB):c.1265C>T (p.Ser422Phe)	rs1057515805	0.00001
NM_001018113.3(FANCB):c.183C>T (p.Ser61=)	rs1317100453	0.00001
NM_001018113.3(FANCB):c.914C>A (p.Ser305Tyr)	rs1057515808	0.00001
NM_001018113.3(FANCB):c.-219G>T	rs373175926
NM_001018113.3(FANCB):c.1078A>G (p.Thr360Ala)	rs956498867
NM_001018113.3(FANCB):c.1652G>A (p.Arg551Lys)	rs2092370985
NM_001018113.3(FANCB):c.1929G>A (p.Glu643=)	rs2092368698
NM_001018113.3(FANCB):c.2373C>T (p.Ser791=)	rs2092363086
NM_001018113.3(FANCB):c.357A>T (p.Glu119Asp)	rs970828551
NM_001018113.3(FANCB):c.782G>A (p.Arg261Gln)	rs1057515809
NM_001018113.3(FANCB):c.809A>G (p.Asn270Ser)	rs2092461325
NM_001018113.3(FANCB):c.952-13C>T	rs1057515807

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