List of variants in gene THRB reported as likely benign for not provided

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001354712.2(THRB):c.1125C>T (p.Ala375=)	rs148991421	0.00033
NM_001354712.2(THRB):c.11A>G (p.Asn4Ser)	rs114070375	0.00028
NM_001354712.2(THRB):c.161C>T (p.Ser54Leu)	rs141731067	0.00018
NM_001354712.2(THRB):c.159G>C (p.Gln53His)	rs567722846	0.00016
NM_001354712.2(THRB):c.40T>C (p.Trp14Arg)	rs777353759	0.00007
NM_001354712.2(THRB):c.129A>T (p.Ser43=)	rs112913751	0.00004
NM_001354712.2(THRB):c.75C>T (p.His25=)	rs760778175	0.00001
NM_001354712.2(THRB):c.22+4T>A	rs1031696535
NM_001354712.2(THRB):c.284-12625C>G

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