List of variants reported as pathogenic for cerebellar ataxia by Breakthrough Genomics, Breakthrough Genomics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000784.4(CYP27A1):c.1420C>T (p.Arg474Trp)	rs121908098	0.00001
NM_020247.5(COQ8A):c.637C>T (p.Arg213Trp)	rs119468005	0.00001
NM_003383.5(VLDLR):c.821-1G>A

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