"GeneDx"[submitter] AND "TSHZ3"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145087	GRCh38/hg38 19q12(chr19:30596523-31293682)x3	LINC01791, LINC01834 +6 more	Copy number gain	See cases	GBenign
Select item 1248896	NM_020856.4(TSHZ3):c.2283T>C (p.Ala761=)	TSHZ3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1241314	NM_020856.4(TSHZ3):c.690G>A (p.Thr230=)	TSHZ3	Single nucleotide variant (synonymous variant)	not provided	GBenign

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