List of variants in gene TRHR reported as likely pathogenic for thyroid gland disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003301.7(TRHR):c.242C>G (p.Pro81Arg)	rs1586182837
NM_003301.7(TRHR):c.343_352delinsA (p.Ser115_Ala118delinsThr)	rs1586182912
NM_003301.7(TRHR):c.597_598del (p.Phe199fs)

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