List of variants reported as likely benign for hyperthyroxinemia by Fulgent Genetics, Fulgent Genetics

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.76G>A (p.Gly26Ser)	rs1800458	0.05309
NM_000371.4(TTR):c.336+18C>T	rs370628373	0.00005
NM_000371.4(TTR):c.-15C>T	rs746692906	0.00003
NM_000371.4(TTR):c.70-20C>T	rs773578107	0.00003
NM_000371.4(TTR):c.78T>C (p.Gly26=)	rs779457244	0.00002
NM_000371.4(TTR):c.121C>A (p.Arg41=)	rs1004021945	0.00001
NM_000371.4(TTR):c.408T>C (p.Tyr136=)	rs1454790119	0.00001
NM_000371.4(TTR):c.40C>T (p.Leu14=)	rs1347695561	0.00001
NM_000371.4(TTR):c.-743A>T	rs3794885
NM_000371.4(TTR):c.141T>C (p.Asn47=)	rs1252826226
NM_000371.4(TTR):c.70-19G>A	rs548935944
NM_000371.4(TTR):c.70-7C>T	rs587780990

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