"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRHR"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055065	NM_003301.7(TRHR):c.9C>T (p.Asn3=)	TRHR	Single nucleotide variant (synonymous variant)	TRHR-related disorder	GLikely benign
Select item 715012	NM_003301.7(TRHR):c.123A>G (p.Val41=)	TRHR	Single nucleotide variant (synonymous variant)	TRHR-related disorder +1 more	GBenign/Likely benign
Select item 3035107	NM_003301.7(TRHR):c.708T>C (p.Asn236=)	TRHR	Single nucleotide variant (synonymous variant)	TRHR-related disorder	GLikely benign

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