List of variants reported as uncertain significance for cerebellar degeneration by Clinical Genetics Laboratory, University Hospital Schleswig-Holstein

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001080414.4(CCDC88C):c.3320ACA[1] (p.Asn1108del)
NM_006796.3(AFG3L2):c.161T>G (p.Leu54Arg)	rs2143234608
NM_015046.7(SETX):c.2114_2118del (p.Ile705fs)
NM_015215.4(CAMTA1):c.241G>A (p.Ala81Thr)
NM_018075.5(ANO10):c.218G>A (p.Gly73Asp)	rs2149481812

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