List of variants reported as pathogenic for familial dysfibrinogenemia by Juno Genomics, Hangzhou Juno Genomics, Inc

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_021871.4(FGA):c.502C>T (p.Arg168Ter)	rs755117226	0.00002
NM_021870.2(FGG):c.902G>A (p.Arg301His)	rs121913088	0.00001
NM_021870.2(FGG):c.901C>T (p.Arg301Cys)	rs121913087
NM_021870.3(FGG):c.1201C>T (p.Arg401Trp)	rs75848804
NM_021870.3(FGG):c.124-2A>G
NM_021871.4(FGA):c.448C>T (p.Gln150Ter)	rs763715993

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