List of variants reported as uncertain significance for autoimmune thyroid disease, susceptibility to by Fulgent Genetics, Fulgent Genetics

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_003235.5(TG):c.848G>A (p.Arg283Gln)	rs146926250	0.00073
NM_003235.5(TG):c.229G>A (p.Gly77Ser)	rs142698837	0.00071
NM_003235.5(TG):c.455G>A (p.Arg152His)	rs114781869	0.00059
NM_003235.5(TG):c.4481C>T (p.Pro1494Leu)	rs146498231	0.00052
NM_003235.5(TG):c.6001G>A (p.Asp2001Asn)	rs199923962	0.00037
NM_003235.5(TG):c.993G>C (p.Gln331His)	rs61745783	0.00028
NM_003235.5(TG):c.1020C>T (p.Asp340=)	rs138114586	0.00021
NM_003235.5(TG):c.2560C>T (p.Arg854Trp)	rs202196940	0.00016
NM_003235.5(TG):c.4982G>A (p.Arg1661His)	rs115509019	0.00012
NM_003235.5(TG):c.3149G>T (p.Trp1050Leu)	rs142124591	0.00007
NM_003235.5(TG):c.2762-4C>T	rs372101475	0.00004
NM_003235.5(TG):c.925A>G (p.Thr309Ala)	rs199712883	0.00002
NM_003235.5(TG):c.385G>A (p.Val129Ile)	rs115677932	0.00001
NM_003235.5(TG):c.3040G>C (p.Asp1014His)	rs114772213
NM_003235.5(TG):c.6131G>T (p.Arg2044Leu)	rs573866267
NM_003235.5(TG):c.7363C>T (p.Arg2455Cys)	rs201444172

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