List of variants in gene FGA reported as likely pathogenic for 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000508.3(FGA):c.92G>T (p.Gly31Val)	rs121909605	0.00001
NM_021871.4(FGA):c.1690_1699dup (p.Ile567fs)	rs1302701490	0.00001
NM_021871.4(FGA):c.364+1G>A	rs778779380	0.00001
NM_000508.3(FGA):c.1717C>T (p.Arg573Cys)	rs121909613
NM_021871.4(FGA):c.1055del (p.Pro352fs)	rs1299596156
NM_021871.4(FGA):c.1339del (p.Glu447fs)
NM_021871.4(FGA):c.1452del (p.Ser485fs)
NM_021871.4(FGA):c.1736dup (p.Tyr579Ter)
NM_021871.4(FGA):c.294_296del (p.Asn99del)
NM_021871.4(FGA):c.607C>T (p.Gln203Ter)
NM_021871.4(FGA):c.713del (p.Lys238fs)
NM_021871.4(FGA):c.922C>T (p.Arg308Ter)	rs776817952

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