List of variants reported as uncertain significance for thyroid gland disorder by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001363711.2(DUOX2):c.1709A>T (p.Gln570Leu)	rs547116063	0.00131
NM_020975.6(RET):c.2261C>T (p.Thr754Met)	rs181856591	0.00009
NM_001354712.2(THRB):c.1354C>A (p.Pro452Thr)	rs2148780678
NM_001363711.2(DUOX2):c.1131G>A (p.Glu377=)
NM_001363711.2(DUOX2):c.3521A>G (p.Lys1174Arg)
NM_001363711.2(DUOX2):c.3968C>T (p.Ala1323Val)	rs78020568
NM_020975.6(RET):c.1142T>G (p.Phe381Cys)

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