List of variants in gene THRB reported as uncertain significance for Thyroid hormone resistance syndrome

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001354712.2(THRB):c.*4477del	rs886058271	0.00001
NM_001354712.2(THRB):c.*1776del	rs536659624
NM_001354712.2(THRB):c.*3879del	rs886058279
NM_001354712.2(THRB):c.3880_3885del	rs886058277
NM_001354712.2(THRB):c.*3880del	rs886058278
NM_001354712.2(THRB):c.3906_3910del	rs559325556
NM_001354712.2(THRB):c.3906_3910dup	rs559325556
NM_001354712.2(THRB):c.3909_3910dup	rs559325556
NM_001354712.2(THRB):c.*3910del	rs559325556
NM_001354712.2(THRB):c.*3910dup	rs559325556
NM_001354712.2(THRB):c.*3915del	rs886058273
NM_001354712.2(THRB):c.*4541dup	rs886058270
NM_001354712.2(THRB):c.4595_4596del	rs886058269
NM_001354712.2(THRB):c.*983TCT[2]	rs886058291
NM_001354712.2(THRB):c.-385GA[1]	rs886058295

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