List of variants in gene THRB reported as uncertain significance 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: 28

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HGVS	dbSNP	gnomAD frequency
NM_001354712.2(THRB):c.532+8G>C	rs146617205	0.00116
NM_001354712.2(THRB):c.52A>C (p.Lys18Gln)	rs141960389	0.00076
NM_001354712.2(THRB):c.213C>A (p.Asp71Glu)	rs141495471	0.00016
NM_001354712.2(THRB):c.1145-5C>T	rs528832730	0.00004
NM_001354712.2(THRB):c.1312C>T (p.Arg438Cys)	rs367757240	0.00001
GRCh37/hg19 3p24.2(chr3:24332058-24456071)x1
GRCh37/hg19 3p24.2(chr3:24459954-24919200)x3
GRCh37/hg19 3p24.2(chr3:24500702-24615559)x3
NM_001354712.2(THRB):c.1022T>C (p.Leu341Pro)	rs2033110557
NM_001354712.2(THRB):c.1028A>C (p.Asn343Thr)	rs1559400861
NM_001354712.2(THRB):c.1039G>T (p.Gly347Trp)
NM_001354712.2(THRB):c.1061T>G (p.Phe354Cys)	rs1559400596
NM_001354712.2(THRB):c.1076C>T (p.Ser359Phe)	rs1553610936
NM_001354712.2(THRB):c.1145A>T (p.Asp382Val)
NM_001354712.2(THRB):c.1147C>T (p.Arg383Cys)	rs1559388949
NM_001354712.2(THRB):c.1335A>T (p.Glu445Asp)	rs1559387816
NM_001354712.2(THRB):c.1336T>G (p.Cys446Gly)
NM_001354712.2(THRB):c.1340C>T (p.Pro447Leu)	rs865994135
NM_001354712.2(THRB):c.1351T>C (p.Phe451Leu)	rs1057519028
NM_001354712.2(THRB):c.1367T>C (p.Leu456Ser)	rs1559387462
NM_001354712.2(THRB):c.1371A>C (p.Glu457Asp)
NM_001354712.2(THRB):c.1377C>A (p.Phe459Leu)	rs2031941762
NM_001354712.2(THRB):c.1A>G (p.Met1Val)	rs886044192
NM_001354712.2(THRB):c.364A>G (p.Ile122Val)	rs2149103720
NM_001354712.2(THRB):c.790G>T (p.Val264Phe)	rs1559415493
NM_001354712.2(THRB):c.958C>A (p.Arg320Ser)	rs121918696
NM_001354712.2(THRB):c.962A>G (p.Tyr321Cys)	rs1559401356
NM_001354712.2(THRB):c.994G>A (p.Gly332Arg)	rs28999969

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