List of variants reported as pathogenic for congenital afibrinogenemia by Fulgent Genetics, Fulgent Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_021871.4(FGA):c.510+1G>T	rs146387238	0.00009
NM_021871.4(FGA):c.502C>T (p.Arg168Ter)	rs755117226	0.00002
NM_021871.4(FGA):c.104G>A (p.Arg35His)	rs121909607	0.00001
NM_021871.4(FGA):c.1634A>T (p.Glu545Val)	rs121909612	0.00001
NM_021871.4(FGA):c.532C>T (p.Arg178Ter)	rs140911890	0.00001
NM_021871.4(FGA):c.117del (p.Val40fs)	rs762964798
NM_021871.4(FGA):c.1541del (p.Pro514fs)

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