List of variants reported as pathogenic for Autosomal dominant cerebellar ataxia, deafness and narcolepsy

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.1532A>G (p.Tyr511Cys)	rs199473690
NM_001130823.3(DNMT1):c.1709C>T (p.Ala570Val)	rs397509392
NM_001130823.3(DNMT1):c.1814G>C (p.Gly605Ala)	rs397509393
NM_001130823.3(DNMT1):c.1816G>T (p.Val606Phe)	rs397509391

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