ClinVar Miner

List of variants reported as likely pathogenic for Autosomal dominant cerebellar ataxia, deafness and narcolepsy by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.1814G>C (p.Gly605Ala)	rs397509393

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