"Diagnostic Laboratory, Department of Genetics, University Medical Cen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 257669	NM_001354712.2(THRB):c.1144+9G>A	THRB	Single nucleotide variant (intron variant)	Thyroid hormone resistance, generalized, autosomal dominant +1 more	GBenign
Select item 198422	NM_001354712.2(THRB):c.735C>T (p.Phe245=)	LOC126806630, THRB	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 1284649	NM_001354712.2(THRB):c.22+4T>A	THRB	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign

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