"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRH"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 260114	NM_007117.5(TRH):c.22C>G (p.Leu8Val)	TRH (L8V)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 3050924	NM_007117.5(TRH):c.105G>A (p.Thr35=)	TRH	Single nucleotide variant (synonymous variant)	TRH-related disorder	GLikely benign
Select item 3041582	NM_007117.5(TRH):c.186G>A (p.Leu62=)	TRH	Single nucleotide variant (synonymous variant)	TRH-related disorder	GLikely benign
Select item 260113	NM_007117.5(TRH):c.212-4C>T	TRH	Single nucleotide variant (intron variant)	Hypothalamic hypothyroidism +2 more	GBenign
Select item 3030548	NM_007117.5(TRH):c.216C>T (p.Ser72=)	TRH	Single nucleotide variant (synonymous variant)	TRH-related disorder	GLikely benign
Select item 260115	NM_007117.5(TRH):c.384T>C (p.Asp128=)	TRH	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 3046852	NM_007117.5(TRH):c.618G>A (p.Ala206=)	TRH	Single nucleotide variant (synonymous variant)	TRH-related disorder	GLikely benign
Select item 260116	NM_007117.5(TRH):c.624T>C (p.Leu208=)	TRH	Single nucleotide variant (synonymous variant)	Hypothalamic hypothyroidism +1 more	GBenign
Select item 260117	NM_007117.5(TRH):c.711A>G (p.Arg237=)	TRH	Single nucleotide variant (synonymous variant)	Hypothalamic hypothyroidism +1 more	GBenign

ClinVar