C3281223[trait identifier] AND "Neurogenetics Research; Murdoch Childr - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 625877	NC_000004.12:g.39348425_39348479delinsAAAGG[400_2000]	RFC1	Indel	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome	GPathogenic
Select item 625876	NC_000004.11:g.39350045_39350099delinsAAGGG[(400_2000)]	RFC1	Indel	Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome	GPathogenic