"GeneDx"[submitter] AND "SUPT5H"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1256822	NM_001111020.3(SUPT5H):c.720G>A (p.Glu240=)	SUPT5H	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1280171	NM_001111020.3(SUPT5H):c.2259-15T>A	SUPT5H	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 253452	GRCh37/hg19 19q13.12-13.2(chr19:37582250-41630908)x3	DPF1, DYRK1B +105 more	Copy number gain	See cases	GPathogenic

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