C1969796[trait identifier] AND "Molecular Genetics, Royal Melbourne Ho - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 450099	NM_006612.6(KIF1C):c.1346A>G (p.Lys449Arg)	KIF1C (K449R)	Single nucleotide variant (missense variant)	Spastic ataxia 2 +2 more	GConflicting classifications of pathogenicity
Select item 450100	NM_006612.6(KIF1C):c.2920G>A (p.Asp974Asn)	KIF1C (D974N)	Single nucleotide variant (missense variant)	Spastic ataxia 2 +2 more	GConflicting classifications of pathogenicity