List of variants reported as likely pathogenic for autosomal dominant cerebellar ataxia by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378969.1(KCND3):c.1070C>T (p.Ser357Leu)	rs867628133
NM_001378969.1(KCND3):c.1129A>G (p.Thr377Ala)
NM_006133.3(DAGLA):c.2437_2446del (p.Leu813fs)

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