List of variants reported as benign for Fanconi anemia complementation group B

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Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_001018113.3(FANCB):c.-173G>C	rs2188383	0.63320
NM_001018113.3(FANCB):c.1327-10T>C	rs2905223	0.53797
NM_001018113.3(FANCB):c.1004G>A (p.Gly335Glu)	rs41309679	0.05446
NM_001018113.3(FANCB):c.*14T>C	rs2375726	0.02466
NM_001018113.3(FANCB):c.-229T>G	rs149617434	0.00830
NM_001018113.3(FANCB):c.402A>G (p.Leu134=)	rs147260208	0.00701
NM_001018113.3(FANCB):c.*66T>G	rs143434225	0.00525
NM_001018113.3(FANCB):c.1996G>A (p.Gly666Ser)	rs145110602	0.00343
NM_001018113.3(FANCB):c.1769T>C (p.Phe590Ser)	rs142959373	0.00109
NM_001018113.3(FANCB):c.*33T>C	rs187611308	0.00068
NM_001018113.3(FANCB):c.1442G>A (p.Arg481His)	rs140198444	0.00053
NM_001018113.3(FANCB):c.69T>C (p.Leu23=)	rs151173533	0.00047
NM_001018113.3(FANCB):c.2452A>G (p.Arg818Gly)	rs143131218	0.00038
NM_001018113.3(FANCB):c.2477C>T (p.Thr826Met)	rs201436396	0.00031
NM_001018113.3(FANCB):c.1371C>T (p.Val457=)	rs149695930	0.00029
NM_001018113.3(FANCB):c.1140T>A (p.Phe380Leu)	rs199909156	0.00020
NM_001018113.3(FANCB):c.2411A>G (p.Asp804Gly)	rs148257882	0.00015
NM_001018113.3(FANCB):c.330A>C (p.Leu110=)	rs201633684	0.00008
NM_001018113.3(FANCB):c.362G>A (p.Arg121His)	rs142289802	0.00008
NM_001018113.3(FANCB):c.1494G>T (p.Lys498Asn)	rs199510538	0.00005
NM_001018113.3(FANCB):c.2165+10A>T	rs184385334	0.00005
NM_001018113.3(FANCB):c.1987A>G (p.Thr663Ala)	rs184796918	0.00003
NM_001018113.3(FANCB):c.1310C>T (p.Thr437Met)	rs772802668	0.00001
NM_001018113.3(FANCB):c.2311A>G (p.Ser771Gly)	rs750381270	0.00001

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