List of variants reported as likely pathogenic for Familial dysfibrinogenemia by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_021870.3(FGG):c.677G>T (p.Gly226Val)	rs1310452604	0.00001
NM_005141.5(FGB):c.498_512del (p.Asn167_Glu171del)
NM_021870.3(FGG):c.1037A>G (p.Asp346Gly)
NM_021871.4(FGA):c.1119G>A (p.Trp373Ter)

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