List of variants in gene FGG reported as other

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
FIBRINOGEN PARIS 1	rs2066862	0.00546
NM_021870.2(FGG):c.1001A>T (p.Asn334Ile)	rs121913090	0.00003
NM_021870.2(FGG):c.902G>A (p.Arg301His)	rs121913088	0.00001
FIBRINOGEN KYOTO 1	rs1578808538
FIBRINOGEN OSLO 3
FIBRINOGEN VLISSINGEN 1
NM_021870.2(FGG):c.1007T>C (p.Met336Thr)	rs121913091
NM_021870.2(FGG):c.1064A>G (p.Gln355Arg)	rs121913092
NM_021870.2(FGG):c.1066G>T (p.Asp356Tyr)	rs121913093
NM_021870.2(FGG):c.1067A>T (p.Asp356Val)	rs121913094
NM_021870.2(FGG):c.1168G>C (p.Asp390His)	rs121913095
NM_021870.2(FGG):c.1201C>G (p.Arg401Gly)	rs75848804
NM_021870.2(FGG):c.901C>T (p.Arg301Cys)	rs121913087
NM_021870.2(FGG):c.926G>A (p.Gly309Asp)	rs121913096
NM_021870.2(FGG):c.952G>C (p.Gly318Arg)	rs267606810
NM_021870.2(FGG):c.953G>T (p.Gly318Val)	rs121913089

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