C3809031[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 55906	NM_007259.5(VPS45):c.671C>A (p.Thr224Asn)	VPS45 (T224N +2 more)	Single nucleotide variant (missense variant +1 more)	Congenital neutropenia-myelofibrosis-nephromegaly syndrome	GPathogenic
Select item 2080467	NM_007259.5(VPS45):c.1129C>A (p.Pro377Thr)	VPS45 (P272T +2 more)	Single nucleotide variant (missense variant +1 more)	Congenital neutropenia-myelofibrosis-nephromegaly syndrome	GUncertain significance