List of variants reported as uncertain significance for cerebellar degeneration by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_006946.4(SPTBN2):c.6736G>A (p.Val2246Met)	rs369469000	0.00001
NM_001080414.4(CCDC88C):c.6035C>T (p.Pro2012Leu)	rs771028975
NM_001080414.4(CCDC88C):c.739G>A (p.Glu247Lys)
NM_001378969.1(KCND3):c.257G>A (p.Arg86Gln)	rs1571941606
NM_004977.3(KCNC3):c.1850C>T (p.Pro617Leu)	rs1284948650
NM_006946.4(SPTBN2):c.7040G>A (p.Arg2347Gln)

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