List of variants in gene FGA reported as benign for coagulation protein disease

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_021871.3(FGA):c.-58A>G	rs2070011	0.65406
NM_021871.4(FGA):c.991A>G (p.Thr331Ala)	rs6050	0.29256
NM_021871.4(FGA):c.16A>G (p.Ile6Val)	rs2070025	0.00250
NM_021871.4(FGA):c.181-14C>T	rs190703077	0.00240
NM_021871.4(FGA):c.300G>A (p.Lys100=)	rs112877216	0.00240
NM_021871.4(FGA):c.904C>G (p.Pro302Ala)	rs200203992	0.00002

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