"Revvity Omics, Revvity"[submitter] AND "DBH"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 365633	NM_000787.4(DBH):c.259T>C (p.Phe87Leu)	DBH (F87L)	Single nucleotide variant (missense variant)	Orthostatic hypotension 1	GUncertain significance
Select item 1750	NM_000787.4(DBH):c.339+2T>C	DBH	Single nucleotide variant (splice donor variant)	not provided +1 more	GPathogenic
Select item 217764	NM_000787.4(DBH):c.1033G>A (p.Asp345Asn)	DBH (D345N)	Single nucleotide variant (missense variant)	Orthostatic hypotension 1	GConflicting classifications of pathogenicity

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