List of variants reported as uncertain significance for familial visceral amyloidosis by Fulgent Genetics, Fulgent Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_004048.4(B2M):c.340A>C (p.Lys114Gln)	rs372078625	0.00011
NM_000039.3(APOA1):c.80C>A (p.Pro27His)	rs121912720	0.00007
NM_000239.3(LYZ):c.175C>T (p.Arg59Ter)	rs374990260	0.00004
NM_021871.4(FGA):c.923G>A (p.Arg308Gln)	rs760992799	0.00004
NM_000239.3(LYZ):c.269G>A (p.Gly90Glu)	rs141911537	0.00003
NM_000039.3(APOA1):c.127G>A (p.Val43Met)	rs373545875	0.00002
NM_000039.3(APOA1):c.168G>A (p.Gln56=)	rs760886281	0.00002
NM_004048.4(B2M):c.278C>A (p.Thr93Asn)	rs778103494	0.00002
NM_021871.4(FGA):c.8C>T (p.Ser3Phe)	rs771156473	0.00002
NM_000039.3(APOA1):c.101G>T (p.Arg34Leu)	rs28929476	0.00001
NM_000039.3(APOA1):c.379G>A (p.Asp127Asn)	rs921646982	0.00001
NM_021871.4(FGA):c.346G>A (p.Asp116Asn)	rs886059153	0.00001
NM_000039.3(APOA1):c.271G>T (p.Val91Leu)	rs2134231457
NM_000239.3(LYZ):c.209C>G (p.Thr70Ser)	rs1349579951
NM_000508.5(FGA):c.2350C>T (p.Gln784Ter)	rs148824832

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