List of variants in gene FGG 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_021870.3(FGG):c.571G>A (p.Gly191Arg)	rs6063	0.00339
NM_021870.3(FGG):c.323C>G (p.Ala108Gly)	rs148685782	0.00222
NM_021870.3(FGG):c.709T>C (p.Tyr237His)	rs762488338	0.00005
NM_021870.3(FGG):c.1099G>A (p.Ala367Thr)	rs78257946	0.00004
NM_021870.2(FGG):c.902G>A (p.Arg301His)	rs121913088	0.00001
NM_021870.3(FGG):c.677G>T (p.Gly226Val)	rs1310452604	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.1006A>T (p.Met336Leu)
NM_021870.3(FGG):c.1030G>C (p.Asp344His)
NM_021870.3(FGG):c.1037A>G (p.Asp346Gly)
NM_021870.3(FGG):c.1067A>G (p.Asp356Gly)
NM_021870.3(FGG):c.124-2A>G
NM_021870.3(FGG):c.207_208dup (p.Glu70fs)	rs2110850824
NM_021870.3(FGG):c.331A>T (p.Lys111Ter)	rs1578812509

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