List of variants in gene THRB reported as likely benign 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001354712.2(THRB):c.*4611del	rs147687234	0.01502
NM_001354712.2(THRB):c.*1750del	rs147125300
NM_001354712.2(THRB):c.*1776dup	rs536659624
NM_001354712.2(THRB):c.*2572ATTG[3]	rs144580659
NM_001354712.2(THRB):c.*3324dup	rs35554555
NM_001354712.2(THRB):c.*570dup	rs569875966
NM_001354712.2(THRB):c.*900del	rs373141874

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