List of variants in gene TG reported as risk factor 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003235.5(TG):c.3082A>G (p.Met1028Val)	rs853326	0.60247
NM_003235.4(TG):c.-1623A>G	rs180195	0.58088
NM_003235.5(TG):c.5995C>T (p.Arg1999Trp)	rs2076740	0.37641
NM_003235.5(TG):c.2200T>G (p.Ser734Ala)	rs180223

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