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

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_021870.3(FGG):c.571G>A (p.Gly191Arg)	rs6063	0.00339
NM_005141.5(FGB):c.794C>T (p.Pro265Leu)	rs6054	0.00275
NM_021870.3(FGG):c.709T>C (p.Tyr237His)	rs762488338	0.00005
NM_005141.5(FGB):c.1330G>A (p.Gly444Ser)
NM_005141.5(FGB):c.419C>A (p.Thr140Asn)
NM_021871.4(FGA):c.103C>G (p.Arg35Gly)	rs121909606

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