List of variants reported as likely benign for Congenital hypothyroidism

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000369.5(TSHR):c.*1154dup	rs3214569	0.85459
NM_003235.5(TG):c.7859G>A (p.Gly2620Asp)	rs978923522	0.00001
NM_001206744.2(TPO):c.2007-9_2007-7del	rs28991288
NM_203395.3(IYD):c.460_461del	rs61597872

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