List of variants reported as likely benign for autosomal dominant cerebellar ataxia by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001128164.2(ATXN1):c.609G>T (p.Gln203His)	rs199744696	0.00060
NM_015215.4(CAMTA1):c.806-11G>A	rs200922493	0.00014
NM_015215.4(CAMTA1):c.4453G>A (p.Glu1485Lys)	rs2096854165

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