List of variants in gene FGA reported as likely benign for familial visceral amyloidosis

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_021871.4(FGA):c.1542T>C (p.Pro514=)	rs4766	0.00426
NM_021871.4(FGA):c.780G>A (p.Glu260=)	rs145563362	0.00167
NM_021871.4(FGA):c.1199C>T (p.Ser400Phe)	rs184635235	0.00031
NM_021871.4(FGA):c.616C>G (p.Gln206Glu)	rs560732073	0.00009
NM_021871.4(FGA):c.1444G>A (p.Val482Met)	rs139146037	0.00006
NM_021871.4(FGA):c.1823G>C (p.Gly608Ala)	rs370873387	0.00006
NM_021871.4(FGA):c.1560C>T (p.Phe520=)	rs778304190	0.00001

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