List of variants in gene FGA studied for Familial dysfibrinogenemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_021871.4(FGA):c.510+1G>T	rs146387238	0.00009
NM_000508.3(FGA):c.103C>T (p.Arg35Cys)	rs121909606	0.00001
NM_021871.4(FGA):c.104G>A (p.Arg35His)	rs121909607	0.00001
NC_000004.11:g.(?_155506411)_(155510715_155511785)del
NC_000004.11:g.(?_155506426)_(155511895_?)del
NM_021871.4(FGA):c.103C>G (p.Arg35Gly)	rs121909606
NM_021871.4(FGA):c.1119G>A (p.Trp373Ter)
NM_021871.4(FGA):c.117del (p.Val40fs)	rs762964798
NM_021871.4(FGA):c.1517del (p.Leu506fs)
NM_021871.4(FGA):c.1754del (p.Ser585fs)
NM_021871.4(FGA):c.448C>T (p.Gln150Ter)	rs763715993
NM_021871.4(FGA):c.541C>T (p.Arg181Ter)

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