List of variants in gene FGG reported as pathogenic for congenital fibrinogen deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
FIBRINOGEN PARIS 1	rs2066862	0.00546
NM_021870.3(FGG):c.323C>G (p.Ala108Gly)	rs148685782	0.00222
NM_021870.2(FGG):c.902G>A (p.Arg301His)	rs121913088	0.00001
NC_000004.11:g.(?_155525322)_(155533809_?)del
NM_021870.2(FGG):c.1007T>C (p.Met336Thr)	rs121913091
NM_021870.2(FGG):c.901C>T (p.Arg301Cys)	rs121913087
NM_021870.3(FGG):c.1022G>A (p.Trp341Ter)	rs1553965519
NM_021870.3(FGG):c.1210T>C (p.Ser404Pro)	rs587777720
NM_021870.3(FGG):c.207_208dup (p.Glu70fs)	rs2110850824
NM_021870.3(FGG):c.307+5G>A	rs587776838
NM_021870.3(FGG):c.331A>T (p.Lys111Ter)	rs1578812509
NM_021870.3(FGG):c.666+23T>A	rs1578810856
NM_021870.3(FGG):c.667-320A>T	rs587776839
NM_021870.3(FGG):c.78+5G>A	rs587776837

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