List of variants reported as likely pathogenic for cerebellar degeneration by Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001032221.6(STXBP1):c.1111-10_1111-6delinsG	rs1588339504
NM_001330260.2(SCN8A):c.2811G>T (p.Trp937Cys)	rs1555225835

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