List of variants reported as likely pathogenic for cerebellar degeneration by Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.2250G>A (p.Lys750=)	rs1137887	0.00003
NM_001134831.2(AHI1):c.1148A>G (p.Asp383Gly)	rs1789162289

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