List of variants in gene TG reported as pathogenic for autoimmune thyroid disease, susceptibility to

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003235.5(TG):c.886C>T (p.Arg296Ter)	rs121912648	0.00041
NM_003235.5(TG):c.4588C>T (p.Arg1530Ter)	rs121912646	0.00011
NM_003235.5(TG):c.6725G>A (p.Arg2242His)	rs2069566	0.00001

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