"GeneDx"[submitter] AND "DRD1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58118	GRCh38/hg38 5q32-35.3(chr5:149714592-181272151)x3	LOC132089226, LOC132089227 +1167 more	Copy number gain	See cases	GPathogenic
Select item 515932	NM_000794.5(DRD1):c.-48=	DRD1	Single nucleotide variant (no sequence alteration)	not specified	GBenign
Select item 511081	NM_000794.5(DRD1):c.-48G>A	DRD1	Single nucleotide variant (5 prime UTR variant)	not specified +1 more	GLikely benign

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