List of variants reported as likely benign 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_021871.4(FGA):c.780G>A (p.Glu260=)	rs145563362	0.00167
NM_004048.4(B2M):c.67+19C>T	rs185185288	0.00091
NM_000039.3(APOA1):c.315C>T (p.Gly105=)	rs148950234	0.00032
NM_004048.4(B2M):c.68-13C>T	rs149900092	0.00032
NM_021871.4(FGA):c.1199C>T (p.Ser400Phe)	rs184635235	0.00031
NM_000039.3(APOA1):c.555G>C (p.Thr185=)	rs143182884	0.00023
NM_000039.3(APOA1):c.200+19G>A	rs377408912	0.00013
NM_000039.3(APOA1):c.726G>C (p.Leu242=)	rs567268961	0.00013
NM_021871.4(FGA):c.1444G>A (p.Val482Met)	rs139146037	0.00006
NM_000239.3(LYZ):c.434G>A (p.Gly145Asp)	rs762616173	0.00004
NM_000039.3(APOA1):c.483G>C (p.Leu161=)	rs747245248	0.00003
NM_000039.3(APOA1):c.126C>T (p.Tyr42=)	rs1591331259	0.00001
NM_004048.4(B2M):c.67+12C>T	rs771780544	0.00001
NM_021871.4(FGA):c.1560C>T (p.Phe520=)	rs778304190	0.00001
NM_000039.3(APOA1):c.162G>C (p.Val54=)	rs193922099

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