List of variants reported as likely pathogenic for hypothyroidism, congenital, nongoitrous by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000369.5(TSHR):c.484C>G (p.Pro162Ala)	rs121908863	0.00010
NM_000369.5(TSHR):c.1170T>G (p.Cys390Trp)	rs121908871	0.00001
NM_000369.5(TSHR):c.1963_1964del (p.Thr655fs)	rs761918916
NM_000369.5(TSHR):c.418del (p.Met140fs)	rs1085307573
NM_004387.4(NKX2-5):c.783del (p.Ala262fs)	rs587784067

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