"Inherited Neuropathy Consortium"[submitter] AND "VRK1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 619020	NM_003384.3(VRK1):c.656G>T (p.Arg219Ile)	VRK1 (R219I)	Single nucleotide variant (missense variant)	Neuronopathy, distal hereditary motor, autosomal recessive 10 +2 more	GConflicting classifications of pathogenicity
Select item 617789	NM_003384.3(VRK1):c.761G>T (p.Trp254Leu)	VRK1 (W254L)	Single nucleotide variant (missense variant)	Neuronopathy, distal hereditary motor, autosomal recessive 10 +2 more	GConflicting classifications of pathogenicity