List of variants in gene FGA reported as uncertain significance 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_021871.4(FGA):c.765G>A (p.Pro255=)	rs779582722	0.00004
NM_021871.4(FGA):c.923G>A (p.Arg308Gln)	rs760992799	0.00004
NM_021871.4(FGA):c.8C>T (p.Ser3Phe)	rs771156473	0.00002
NM_000508.5(FGA):c.2089G>A (p.Gly697Ser)	rs771023837	0.00001
NM_021871.4(FGA):c.1025G>A (p.Gly342Glu)	rs774664670	0.00001
NM_021871.4(FGA):c.1615G>A (p.Glu539Lys)	rs1190260696	0.00001
NM_021871.4(FGA):c.1760C>G (p.Thr587Arg)	rs1309799184	0.00001
NM_021871.4(FGA):c.346G>A (p.Asp116Asn)	rs886059153	0.00001
NM_021871.4(FGA):c.822C>T (p.Ser274=)	rs886059150	0.00001
NM_021871.4(FGA):c.919A>G (p.Asn307Asp)	rs750564329	0.00001
NM_000508.5(FGA):c.2350C>T (p.Gln784Ter)	rs148824832
NM_021871.4(FGA):c.1120A>G (p.Thr374Ala)
NM_021871.4(FGA):c.1207G>A (p.Ala403Thr)	rs1730710209
NM_021871.4(FGA):c.1621G>C (p.Val541Leu)	rs1578795080
NM_021871.4(FGA):c.215G>A (p.Gly72Glu)	rs1730803914
NM_021871.4(FGA):c.614A>G (p.Glu205Gly)	rs886059152
NM_021871.4(FGA):c.666A>T (p.Pro222=)	rs886059151

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