List of variants in gene THRB reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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_001354712.2(THRB):c.*4G>A	rs777224982	0.00003
NM_001354712.2(THRB):c.1293A>G (p.Ile431Met)	rs1553609195
NM_001354712.2(THRB):c.920G>A (p.Gly307Asp)	rs1553611101

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