List of variants reported as likely benign for thyroid hormone resistance syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_003466.4(PAX8):c.985T>C (p.Phe329Leu)	rs3188996	0.01628
NM_004387.4(NKX2-5):c.852C>G (p.Ala284=)	rs374150672	0.00023
NM_004387.4(NKX2-5):c.823C>A (p.Pro275Thr)	rs368366482	0.00013
NM_004387.4(NKX2-5):c.492G>C (p.Ser164=)	rs754229011	0.00006
NM_004387.4(NKX2-5):c.609G>A (p.Glu203=)	rs376792087	0.00006
NM_001354712.2(THRB):c.175A>G (p.Ile59Val)	rs141172732	0.00003

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