List of variants reported as uncertain significance for congenital afibrinogenemia by ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_005141.5(FGB):c.794C>T (p.Pro265Leu)	rs6054	0.00275
NM_005141.5(FGB):c.656A>G (p.Gln219Arg)	rs778766319	0.00001
NM_005141.5(FGB):c.506T>A (p.Val169Asp)	rs2110768107
NM_005141.5(FGB):c.946T>C (p.Cys316Arg)
NM_021870.3(FGG):c.793C>T (p.Gln265Ter)	rs771279321
NM_021871.4(FGA):c.1486G>T (p.Asp496Tyr)	rs2110809573
NM_021871.4(FGA):c.364+5G>A	rs891744509

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