List of variants in gene THRB reported as pathogenic by GeneDx

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001354712.2(THRB):c.1313G>A (p.Arg438His)	rs121918698	0.00001
NM_001354712.2(THRB):c.1302C>A (p.Cys434Ter)	rs121918705
NM_001354712.2(THRB):c.1336T>C (p.Cys446Arg)	rs121918703
NM_001354712.2(THRB):c.1357C>A (p.Pro453Thr)	rs28933408
NM_001354712.2(THRB):c.949G>A (p.Ala317Thr)	rs121918690
NM_001354712.2(THRB):c.958C>T (p.Arg320Cys)	rs121918696
NM_001354712.2(THRB):c.959G>A (p.Arg320His)	rs121918693

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