List of variants reported as likely pathogenic for cerebellar ataxia by NIHR Bioresource Rare Diseases, University of Cambridge

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000303.3(PMM2):c.422G>A (p.Arg141His)	rs28936415	0.00338
NC_012920.1(MT-ATP6):m.9032T>C	rs1603221994
NM_000303.3(PMM2):c.584A>G (p.His195Arg)	rs1596489887

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