"Diagnostic Laboratory, Department of Genetics, University Medical Cen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 845618	NM_006612.6(KIF1C):c.1165+3C>T	KIF1C	Single nucleotide variant (intron variant)	Spastic ataxia 2	GUncertain significance
Select item 390925	NM_006612.6(KIF1C):c.3071G>A (p.Arg1024Gln)	KIF1C (R1024Q)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia +3 more	GLikely benign