List of variants reported as likely pathogenic for cerebellar degeneration by Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015046.7(SETX):c.5332C>T (p.Arg1778Ter)	rs1169623576	0.00001
NM_001961.4(EEF2):c.2314G>A (p.Glu772Lys)	rs2145355764
NM_005861.4(STUB1):c.784C>T (p.Gln262Ter)
NM_014363.6(SACS):c.5972dup (p.Arg1992fs)	rs2137613912

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