List of variants reported as uncertain significance for Hyperthyroxinemia, dystransthyretinemic; Amyloidosis, hereditary systemic 1; Carpal tunnel syndrome 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.190T>C (p.Phe64Leu)	rs138065384	0.00019
NM_000371.4(TTR):c.368G>A (p.Arg123His)	rs148538950	0.00019
NM_000371.4(TTR):c.14G>A (p.Arg5His)	rs138657343	0.00017
NM_000371.4(TTR):c.235A>G (p.Thr79Ala)	rs770389488	0.00015
NM_000371.4(TTR):c.-61G>A	rs770403822	0.00014
NM_000371.4(TTR):c.140A>G (p.Asn47Ser)	rs145551875	0.00010
NM_000371.4(TTR):c.*143G>C	rs545271394	0.00008
NM_000371.4(TTR):c.280G>C (p.Asp94His)	rs730881164	0.00007
NM_000371.4(TTR):c.13C>T (p.Arg5Cys)	rs144792001	0.00005
NM_000371.4(TTR):c.370C>T (p.Arg124Cys)	rs745834030	0.00005
NM_000371.4(TTR):c.361G>A (p.Gly121Ser)	rs755337715	0.00004
NM_000371.4(TTR):c.385G>A (p.Ala129Thr)	rs267607159	0.00004
NM_000371.4(TTR):c.209G>A (p.Ser70Asn)	rs121918080	0.00002
NM_000371.4(TTR):c.439G>T (p.Glu147Ter)	rs730881162	0.00002
NM_000371.4(TTR):c.127A>C (p.Ser43Arg)	rs11541800	0.00001
NM_000371.4(TTR):c.136A>G (p.Ile46Val)	rs773584864	0.00001
NM_000371.4(TTR):c.151C>A (p.His51Asn)	rs915983905	0.00001
NM_000371.4(TTR):c.200+4A>G	rs751512499	0.00001
NM_000371.4(TTR):c.263T>C (p.Ile88Thr)	rs1567946180	0.00001
NM_000371.4(TTR):c.301G>A (p.Ala101Thr)	rs730881165	0.00001
NM_000371.4(TTR):c.314C>T (p.Ser105Phe)	rs1322942118	0.00001
NM_000371.4(TTR):c.406T>C (p.Tyr136His)	rs766909913	0.00001
NM_000371.4(TTR):c.68C>T (p.Thr23Met)	rs377052919	0.00001
NM_000371.4(TTR):c.11_13del (p.His4del)	rs747545126
NM_000371.4(TTR):c.11_13dup (p.His4dup)	rs747545126
NM_000371.4(TTR):c.37G>A (p.Gly13Arg)	rs767889884
NM_000371.4(TTR):c.83C>T (p.Ser28Phe)	rs1313375879
NM_000371.4(TTR):c.88T>G (p.Cys30Gly)	rs121918083

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