List of variants reported as pathogenic for thyroid gland disorder by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001363711.2(DUOX2):c.1462G>A (p.Gly488Arg)	rs191759494	0.00024
NM_000369.5(TSHR):c.1349G>A (p.Arg450His)	rs189261858	0.00023
NM_020975.6(RET):c.2410G>A (p.Val804Met)	rs79658334	0.00022
NM_020975.6(RET):c.1998G>T (p.Lys666Asn)	rs146646971	0.00003
NM_020975.6(RET):c.1826G>A (p.Cys609Tyr)	rs77939446	0.00001
NM_020975.6(RET):c.1900T>C (p.Cys634Arg)	rs75076352	0.00001
NM_020975.6(RET):c.2671T>G (p.Ser891Ala)	rs75234356	0.00001
NM_001363711.2(DUOX2):c.2895_2898del (p.Phe966fs)	rs530719719
NM_003235.5(TG):c.5184C>A (p.Cys1728Ter)	rs199599591
NM_020975.6(RET):c.1858T>C (p.Cys620Arg)	rs77316810
NM_020975.6(RET):c.1858T>G (p.Cys620Gly)	rs77316810

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