List of variants reported as likely pathogenic for thyroid cancer, nonmedullary, 1

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_021930.6(RINT1):c.1107+1G>T	rs200989342	0.00001
NM_001079668.3(NKX2-1):c.572G>T (p.Arg191Leu)
NM_004985.5(KRAS):c.445A>T (p.Arg149Ter)	rs2141505552
NM_021930.6(RINT1):c.1021C>G (p.Leu341Val)	rs151055286
NM_206937.2(LIG4):c.1673A>C (p.Gln558Pro)	rs751409106

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