List of variants in gene combination LOC126806630, THRB reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001354712.2(THRB):c.679_696dup (p.Glu227_Thr232dup)	rs1553616532
NM_001354712.2(THRB):c.700G>C (p.Ala234Pro)	rs121918694
NM_001354712.2(THRB):c.727C>G (p.Arg243Gly)	rs121918707
NM_001354712.2(THRB):c.737T>C (p.Leu246Pro)	rs1553616482

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