List of variants reported as likely pathogenic for Congenital nongoitrous hypothyroidism 6

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_199334.5(THRA):c.1141C>T (p.His381Tyr)
NM_199334.5(THRA):c.518A>G (p.Glu173Gly)	rs1987264133
NM_199334.5(THRA):c.788C>T (p.Ala263Val)	rs1555545033
NM_199334.5(THRA):c.818C>A (p.Thr273Asn)	rs2145085082
NM_199334.5(THRA):c.896T>C (p.Ile299Thr)

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